FDA Inspection
Regeneron Pharmaceuticals IncRegeneron Pharmaceuticals Inc – FDA Inspection, Aug 19, 2016
Record Details
This FDA Inspection record concerns Regeneron Pharmaceuticals Inc, with an inspection on August 19, 2016, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- August 19, 2016
- Product Type
- Drugs
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ID · caf7d10a-59bc-40a1-b6f6-8e3e13e51b49
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 983604
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Regeneron Pharmaceuticals Inc
12| Date | Classification | Office | Project area |
|---|---|---|---|
| March 22, 2024 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| February 16, 2024 | Not classified | New York District Office | |
| October 25, 2021 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 18, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| June 8, 2018 | Not classified | New York District Office |
Other documents for Regeneron Pharmaceuticals Inc
- FDA Inspection 1230565 - 2024-03-22
- FDA Inspection 1239760 - 2024-02-16
- FDA Inspection 1155063 - 2021-10-25
- FDA Inspection 1106821 - 2019-10-18
- FDA Inspection 1059234 - 2018-06-08
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