FDA Inspection
Pfizer, Inc.Pfizer, Inc. – FDA Inspection, Jun 6, 2012
Record Details
This FDA Inspection record concerns Pfizer, Inc., with an inspection on June 6, 2012, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Pfizer, Inc.
- Inspection Date
- June 6, 2012
- Product Type
- Drugs
View Company Profile
ID · 9fdf0404-f92b-4ca1-8d79-108e5af35674
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 785216
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 312.50Ensuring compliance with plan and protocol
- 21 CFR 312.55(b)New observations, adverse effects and risks
Full citation text and observation details available on the Dashboard.
Other FDA inspections of Pfizer, Inc.
25| Date | Classification | Office | Project area |
|---|---|---|---|
| October 24, 2025 | Not classified | New England District Office | |
| December 13, 2024 | VAI | New England District Office | Bioresearch Monitoring: Human Drugs |
| August 30, 2024 | Not classified | New England District Office | |
| July 19, 2024 | Not classified | New England District Office | |
| April 19, 2023 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Pfizer, Inc.
- FDA Inspection 1284680 - 2025-10-24
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- FDA Inspection 1249289 - 2024-08-30
- FDA Inspection 1230476 - 2024-07-19
- FDA Inspection 1204434 - 2023-04-19
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