FDA freedom of information request on inspections carried out on Pfizer's Wyeth Biopharma

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Why a FOI request to the FDA?

Wyeth BioPharma is the manufacturer of the Pfizer/BioNTech covid injections, code named BNT162b2. It is a US-based company and its inspection record is available on the FDA website. This is the subject of the FOI, with the link to the FDAs reply:

Inspection at FEI Number 1222181, Wyeth BioPharma Division of Wyeth Pharmaceuticals

You can click on the link to read the letter, or this is the main body of the text:

“Dear Requester:

The Food and Drug Administration (FDA) has received your Freedom of Information Act (FOIA) request for records regarding:

This FOI relates to the following Inspection at FEI Number 1222181, Wyeth BioPharma Division of Wyeth Pharmaceuticals:

Inspection End Date: 09/19/2023 Inspection ID: 1218069 Product Type: Biologics Classification: VAI. (Voluntary Action Initiated).

I wish to know what the voluntary action comprised and would like sight of the inspection report, if that were possible. Was there a further FDA inspection (biologics) to co…