Published: January 3, 2022
By: Mark Wallace
On Thursday, a Federal Judge “soundly” rejected the FDA’s panicked request for permission to produce hundreds of thousands of documents related to Pfizer and the Covid vaccines at a rate of 500 pages per month after the agency was ordered to comply with a Freedom of Information Act (FOIA) request last month.
The FDA’s unbelievable request would have allowed them to take an unbelievable 55 years to produce all of the documents.
But thanks to Texas Northern District Judge Mark Pittman’s ruling, the agency will be forking those likely damning records over within the next few months, at a rate of 55,000 every 30 days.
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The first deadline, which is on January 31st, requires the FDA to turn over 12,000 pages, with the rest coming monthly after that.
From Pittman’s decision:
“Accordingly, the Court concludes that this FOIA request is of paramount public importance.
‘Stale information is of little value’ – the Court, agreeing with this truism, therefore concludes that the expeditious completion of Plaintiff’s request is not only practicable, but necessary.
To that end, the Court further concludes that the production rate, as detailed below, appropriately balances the need for unprecedented urgency in processing this request with the FDA’s concerns regarding the burdens of production.
The FDA shall produce the “more than 12,000 pages” articulated in its own proposal, see ECF No. 29 at 24, on or before January 31, 2022.
The FDA shall produce the remaining documents at a rate of 55,000 pages every 30 days, with the first production being due on or before March 1, 2022, until production is complete.”
Wow. Considering what we got out of the first batch of documents, which was just 500 pages – you can bet there will be some damning data coming soon.
Aaron Siri, who is one of the lawyers working to process the FOIA request, announced the huge news on his Substack channel, calling it a “great win for transparency” and a huge step towards holding the corrupt public health bureaucracy accountable for hiding the data about the dangerousness of the experimental Covid vaccines from the public.
“This is a great win for transparency and removes one of the strangleholds federal “health” authorities have had on the data needed for independent scientists to offer solutions and address serious issues with the current vaccine program – issues which include waning immunity, variants evading vaccine immunity, and, as the CDC has confirmed, that the vaccines do not prevent transmission.
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