FDA Inspection
Pfizer Inc.Pfizer Inc. – FDA Inspection, Aug 26, 2015
Record Details
This FDA Inspection record concerns Pfizer Inc., with an inspection on August 26, 2015, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Pfizer Inc.
- Inspection Date
- August 26, 2015
- Product Type
- Drugs
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ID · db0e128d-dba7-43d8-ba7e-816e03528044
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 946884
- FDA center
- Human Drugs
- Project area
- Bioresearch Monitoring
FDA Citations
2- 21 CFR 314.80(j)Failure to maintain records
- 21 CFR 314.80(b)Failure to develop written procedures
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Other FDA inspections of Pfizer Inc.
4| Date | Classification | Office | Project area |
|---|---|---|---|
| July 22, 2022 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| October 15, 2012 | VAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| June 6, 2012 | NAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
| August 10, 2009 | OAI | Center for Drug Evaluation and Research | Bioresearch Monitoring |
Other documents for Pfizer Inc.
- FDA Inspection 1176364 - 2022-07-22
- FDA Inspection 805292 - 2012-10-15
- FDA Inspection 785976 - 2012-06-06
- FDA Inspection 606526 - 2009-08-10
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