How the FDA extorts money from nutritional supplement companiesThe FDA extortion racket works like this: FDA employees use keyword-scanning software to scan the web pages of natural health product and supplement companies, searching for terms like cancer, cures, treatment, remedies and other "forbidden" words. FDA employees then review the discovered pages to determine if they contain any words that might inform consumers of the health benefits of the nutritional products. FDA employees also look for links that might point web users to scientific articles from peer-reviewed medical journals that further explain the health benefits of specific foods, supplements or nutrients.
When offending words or links are found by the FDA, their extortion team goes into full swing. First, they contact the company and warn them to remove all information and links from their websites. This is the most important step from the FDA's standpoint, because by doing this, they can keep the health-conscious public in a state of nutritional ignorance about the scientifically-supported healing properties of natural supplements. Cherry products, for example, cannot link to scientific articles explaining the simple biological fact that cherries ease inflammation in human beings. Such links are considered "drug claims" by the FDA.
Companies are now being targeted for simply posting customer testimonials, even when those testimonials make absolutely no health claims. FDA and FTC agents are now threatening the owners of such companies with imprisonment if they do not immediately remove all customer testimonials from their websites and marketing materials.
If the company being targeted for extortion refuses to fully comply with the FDA's requests to remove all educational information from their website, the FDA then escalates the extortion tactics by threatening the company principals with arrest and seizure unless they agree to pay hundreds of thousands of dollars to top FDA contractors and sign a "consent decree" where the company "admits" to committing various crimes (see below). This consent decree is a blatant violation of the Constitutional rights of U.S. citizens, of course, and it violates numerous sections of the Bill of Rights (Amendments #1 and #5, at the very least).
The FDA employees or contractors receiving the extorted money, it is claimed, are being paid to "review web pages" to make sure they don't contain anything that might inform consumers about the scientifically-validated benefits of the health products being sold. FDA extortion agreements specify that FDA employees should be paid the rate of $100 per hour, with no limit on the number of hours they may bill the company for. The extortion agreement also requires companies to pay for all the following:
• $100 per hour for the travel time of FDA employees.
• Hotel rooms for FDA employees.
• Storage fees for all products seized by the FDA.
The same agreement also requires the company to comply with FDA demands by never placing any links or "illegal" information on its website, where "illegal" means anything that offers an accurate description of the health benefits offered by natural health products.
The Consent DecreePart of the FDA's strategy for oppression and control is to force targeted companies to sign a "consent decree" where they admit to crimes they never committed. NaturalNews obtained a copy of a public court document the FruitFast company was forced to sign due to FDA threats and extortion tactics.
You can view this document yourself at: http://www.NaturalNews.com/investigatio...
This document requires the FruitFast company to admit to crimes it did not commit; namely:
"Violating the Act, by introducing or delivering for introduction, or causing to be introduced or delivered for introduction, into interstate commerce articles of drug that are misbranded within the meaning of 21 U.S.C. SS 352(f)(1)."
What "drugs" did the FruitFast company introduce that were "misbranded?" Cherries, it turns out. Cherry juice concentrate was being sold with the accurate statement that it helped eliminate gout (which it does). This, according to the FDA, was enough to magically transform cherry juice into an "unapproved drug" and cause it to be "misbranded."
It also requires targeted companies to contractually agree that they have:
"...removed all claims from Defendants' product labels, labeling, promotional materials, websites owned or controlled by Defendants, and in any other media that cause that product to be a drug and/or contain unapproved or unauthorized health claims within the meaning of the Act; and
(ii) removed, from their product labels, labeling, promotional materials, and websites owned or controlled by Defendants, references to or endorsements of any other website that conveys information about Defendants' products that cause those products to be a drug and/or contain unapproved or unauthorized health claims within the meaning of the Act."
This means, of course, that these companies can no longer even LINK to other websites, including websites of scientific journals that discuss the proven health benefits of such natural products (foods, herbs, etc.)
The truth is now subject to FDA approvalOnce a company removes all educational information and links from their website, they are then required to submit to draconian measures of "censorship enforcement" by the FDA. This is fully explained in this section of the FDA's Consent Decree: (bolding added for emphasis)
Within ten (10) calendar days of FDA's request for any labels, labeling, promotional materials, and/or downloaded copies (on CD-Rom) of any internet websites owned or controlled by Defendants or websites referenced by, endorsed, or adopted directly or indirectly by Defendants, Defendants shall submit a copy of the requested materials to FDA at the address specified in paragraph 19.
Within twenty (20) calendar days of entry of this Decree, Defendants shall submit to FDA a certification of compliance, signed by each of the individually-named Defendants in this matter, each Defendant stating that he: (a) has personally reviewed all of Defendants' product labels, labeling, promotional materials, and the internet websites referred to in paragraph 8 above; and (b) personally certifies that the product labels, labeling, promotional materials, and internet websites strictly comply with the requirements of the Act and its regulations and do not include unapproved or unauthorized claims that the products cure, mitigate, treat, prevent and/or reduce the risk of disease. Thereafter, Defendants shall submit certifications of compliance every three (3) months for a period of two (2) years.
Furthermore, the FDA then requires that the company being targeted by the extortion racket hire a person (called the "expert") to enforce all this censorship the company has agreed to.
As you'll note in the language below, this "expert" must be paid $100 an hour, for an unlimited number of hours, to conduct surprise inspections of the company's administrative offices, warehouses and fulfillment centers:
Within fourteen (14) calendar days of entry of this Decree, Defendants shall retain an independent person or persons (the "expert")... who by reason of background, experience, education, and training is qualified to assess Defendants' compliance with the Act, to review the claims Defendants make for all of their products on their product labels, labeling, promotional material, any internet websites owned or controlled by Defendants, including, but not limited to, the websites referred to in paragraph 8 above. At the conclusion of the expert's review, the expert shall prepare a written report analyzing whether Defendants are operating in compliance with the Act and in particular, certify whether Defendants have omitted all claims from their product labels, labeling, promotional materials, websites owned or controlled by Defendants, and in any other media, that make any of their products drugs and/or constitute unapproved or unauthorized health claims within the meaning of the Act. The expert shall also review Defendants' product labels, labeling, promotional materials, and websites owned or controlled by Defendants to determine whether these include any references to or endorsements of any other websites that convey information about Defendants' products that cause those products to be a drug and/or contain unapproved or unauthorized health claims within the meaning of the Act, and certify in the written report whether Defendants have omitted any such references or endorsements. The expert shall submit this report to FDA and Defendants within thirty-five (35) calendar days of the entry of this Decree. If the expert reports any violations of the Act, Defendants shall, within seven (7) calendar days of receipt of the report, correct those deviations, unless FDA notifies Defendants that a shorter time period is necessary.
In other words, this section requires the company being targeted to pay the "Expert" huge fees to make sure it doesn't "illegally" link to other websites that might tell the truth about the health products in question.
FDA tyranny unleashedSo what happens if the company slips up and does something illegal like, let's say, posting a clickable link to a science journal that discusses research citing the health benefits of cherries? As you'll see below, there are no limits to the action the FDA can take in retribution, including the seizure of all company assets and the arrest of its principals.
Specifically, the Consent Decree forces company owners to agree to the following:
If, at any time after this Decree has been entered, FDA determines, based on the results of an inspection, the analyses of Defendants' product labels, labeling, promotional materials, websites owned or controlled by Defendants, or websites referenced by, endorsed, or adopted directly or indirectly by Defendants that convey information about Defendants' products, a report prepared by Defendants' expert, or any other information, that additional corrective actions are necessary to achieve compliance with the Act, applicable regulations, or this Decree, FDA may, as and when it deems necessary, direct Defendants, in writing, to take one or more of the actions:
A. Cease manufacturing, processing, packing, labeling, holding, and/or distributing any article(s);
B. Submit additional reports or information to FDA;
C. Recall any article(s) at Defendants' expense; or
D. Take any other reasonable corrective action(s) as FDA, in its discretion, deems necessary to bring Defendants and their products into compliance with the Act, applicable regulations, and this Decree.
Surprise inspections, secret police and non-stop persecutionJust to keep the targeted company in a state of constant fear (which is why I have labeled the FDA a terrorist organization), the FDA forces it to agree to surprise inspections where it must pay FDA "compliance officers" to rummage through their product shelves and paperwork, looking for evidence of non-compliance:
Duly authorized representatives of FDA shall be permitted, without prior notice and as and when FDA deems necessary, to make [surprise] inspections of Defendants' facilities and, without prior notice, take any other measures necessary to monitor and ensure continuing compliance with the terms of this Decree. During such inspections, FDA representatives shall be permitted prompt access to buildings, equipment, in-process and finished materials, containers, labeling and other materials therein; to take photographs and make video recordings; to take samples of Defendants' finished and unfinished materials and products, containers, labels, labeling, and other promotional materials; and to examine and copy all records relating to the receipt, manufacture, processing, packing, labeling, promoting, holding, and distribution of any and all Defendants' products in order to ensure continuing compliance with the terms of this Decree. The inspections shall be permitted upon presentation of a copy of this Decree and appropriate credentials. The inspection authority granted by this Decree is separate from, and in addition to, the authority to conduct inspections under the Act, 21 U.S.C. §374.
And just to make sure the company is further driven into bankruptcy, the FDA requires them to PAY for all these surprise "compliance" investigations! As stated in the Consent Decree:
Defendants shall reimburse FDA for the costs of all FDA inspections, investigations, supervision, reviews, examinations, and analyses specified in this Decree or that FDA deems necessary to evaluate Defendants' compliance with this Decree. The costs of such inspections shall be borne by Defendants at the prevailing rates in effect at the time the costs are incurred. As of the date that this Decree is signed by the parties, these rates are:$78.09 per hour and fraction thereof per representative for inspection work; $93.61 per hour or fraction thereof per representative for analytical or review work; $0.485 per mile for travel expenses by automobile; government rate or the equivalent for travel by air or other means; and the published government per diem rate or the equivalent for the areas in which the inspections are performed per-day, per-representative for subsistence expenses, where necessary. In the event that the standard rates applicable to FDA supervision of court-ordered compliance are modified, these rates shall be increased or decreased without further order of the Court."
Are you getting the picture here? The FDA can simply show up on a "surprise" inspection, bring ten FDA agents, bill the company for thousands of hours, and bankrupt the company while padding its own pockets.
Doesn't this sound a lot like the King's Consent Decree against the American colonies? The FDA's agreement reads amazingly like a document a King might force his subjects to sign as he's taking over their land and gold, imprisoning them in his kingdom.
But it gets better: The FDA also requires the Defendants to reveal all sorts of details about their business operations:
"Within ten (10) calendar days of entry of this Decree, Defendants shall provide FDA a list of all domain names and IP addresses they use to market or describe any product, regardless of whether such sites mention specific products Defendants sell.
Defendants shall notify the District Director, FDA Detroit District Office, in writing at least fifteen (15) calendar days before any change in ownership, character, or name of its business.
If Defendants fail to comply with any of the provisions of this Decree, including any time frame imposed by this Decree, then, on motion of the United States in this proceeding, Defendants Brownwood Acres and/or Cherry Capital shall pay to the United States of America the sum of one thousand dollars ($1,000) in liquidated damages per violation per day so long as such violation continues.
Should the United States bring, and prevail in, a contempt action to enforce the terms of this Decree, Defendants shall, in addition to other remedies, reimburse the United States for its attorneys* fees, investigational expenses, expert witness fees, travel expenses incurred by attorneys and witnesses, and administrative court costs relating to such contempt proceedings.
And finally, just to make sure everybody knows who's in charge, here's what the agreement says about final judgment:
All decisions specified in this Decree shall be vested in the discretion of FDA and shall be final.
In other words, the FDA is the King. It is above the law. It answers to no one but itself.
Welcome to the United States of Tyranny, FDA style.
The full text of the FDA's agreement, including the names of the top FDA criminals who signed it, is included at the end of this article.
This brand of tyranny is reserved for health supplement companiesWhile the FDA gives drug companies a free pass of easy approval for dangerous drugs, this Consent Decree is the kind of treatment it slams down upon health product companies. As you can see from the text in the decree, above, this is a document of outright tyranny and oppression.
Any company signing this document gives the FDA all the tools it needs to drive that company completely out of business. Sadly, dozens of companies have signed this in just the last year. The FDA's reign of terror is working. It's putting health companies out of business and forcing them to censor themselves. It even forces them toremove all web links to information sources like NaturalNews.com or peer-reviewed science journals.
This is all part of the FDA's campaign of health illiteracy -- a war of disinformation being waged against the American people. It is a secret war being fought out of the view of the mainstream media (which refuses to report this story) and far from the scrutiny of the U.S. Dept. of Justice (which doesn't care about the real tyrants running loose in this country).
The FDA is an out-of-control, rogue agency engaged in acts of deception against the American people. By itself, it is negligent in the deaths of tens of millions of Americans, and it has taken it upon itself to increase the body count by making sure consumers have zero access to honest, truthful, scientifically-validated information about the healing properties of health supplements.
The FDA, by any account, is a much greater threat to the health and safety of the American people than any terrorist group, and if the U.S. really wanted to fight terror and tyranny, it would start by arresting top FDA officials at gunpoint. Those targeted for arrest and prosecution should also include the lawyers and paper pushers involved in this very agreement (see their names on the legal documents at the end of this article).
In my view, these people are the real criminals at work here. They are the masterminds of this campaign of extortion and terror being leveled against health companies by the rogue U.S. Food and Drug Administration. Much like Hitler's top generals, they play an important role in the mass disinformation that's resulting in the needless death of millions of people. By any account, they are all guilty of crimes against humanity and should be arrested and prosecuted as such. We should all be so fortunate to live to the day where we can see these white-collar criminals behind bars, perhaps sharing their jail cells with other war criminals from the Bush Administration.
Sign this or you'll be arrestedWhat you haven't yet seen in all this is the barrage of threats leveled against companies if they don't sign this Consent Decree! Company executives receive both written and verbal threats from top FDA "enforcement officers" who claim they will "throw you in prison" if you don't sign the agreement.
Every major health trade show is forced to hire a FDA compliance officer ( Nazi Storm Trooper) whose job it is to walk the show floor and threaten companies into compliance. This includes shows like Expo West and Expo East, where show organizers also serve as de facto FDA agents themselves, barring the participation of exhibitors who dare to tell the truth about their natural products. This smacks of KGB secret police operations in the former Soviet Union. But secret FDA police are now a reality in the United States of America.
There has been reported numerous verbal threats from FDA compliance officers directed at health supplement companies during trade shows, including threats to "put you out of business," "throw you in prison" or "take every last dollar you've ever earned."
FDA compliance officers are the foot soldiers of the agency's war against the truth. They seek out any health claim that might inform consumers about the properties of nutritional supplements, then they work to squash such statements before they become too well known. In essence, they are censorship officers who enforce nutritional illiteracy and prevent knowledge from being shared.
As such, they are acting not merely as secret police on a mission to destroy small American businesses; they are actually agents of disinformation, bent on destroying knowledge and enforcing a system of mandatory ignorance. This is entirely consistent with the FDA's history of ordering the destruction of recipe books that promoted the use of the natural herb stevia, among many other examples of information suppression.
The FDA's campaign of health illiteracy and enforced ignoranceIt is the FDA's position that there is no such thing as any food, beverage, supplement or herb that has any health benefit whatsoever. Merely making such a claim instantly qualifies your product as a "new and unapproved drug," according to the FDA.
Officially, the FDA claims all health products are inert and have no properties other than their macronutrients (fiber, carbohydrates, protein, etc.).
There is only one class of substances that has
any beneficial biological effect on the human
body, the FDA states that is: Pharmaceuticals.
Only those patented, synthetic chemicals are allowed to be described as having benefits to human health.
This convenient position is entirely consistent with the protection of the profits of drug companies. It's no coincidence that the drug companies fund the FDA through "user fees," and most FDA employees are dependent on drug company money... except, of course, those FDA people earning their living by extorting millions of dollars from health product companies.
The upshot of the FDA's campaign against health supplements is that most of the American people remain nutritionally illiterate, oblivious to the scientifically-validated health benefits offered by tens of thousands of different nutrients, plants, supplements and products. To say that zinc speeds healing, or that vitamin D prevents cancer, or that resveratrol lowers high cholesterol is common sense in the scientific community, but it's a crime in the eyes of the FDA.