FDA Inspection
Teva Branded Pharmaceutical Products R&D, LLCTeva Branded Pharmaceutical Products R&D, LLC – FDA Inspection, May 15, 2017
Record Details
This FDA Inspection record concerns Teva Branded Pharmaceutical Products R&D, LLC, with an inspection on May 15, 2017, issued by the Philadelphia District Office, covering human drugs.
- Inspection Date
- May 15, 2017
- Product Type
- Human Drugs
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ID · 4a903353-5518-44b7-8ea8-464d714ee19c
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1017798
- FDA center
- Human Drugs
- Project area
- Generic Drug Evaluation
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.160(b)Scientifically sound laboratory controls
- 21 CFR 211.192Investigations of discrepancies, failures
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Other FDA inspections of Teva Branded Pharmaceutical Products R&D, LLC
1| Date | Classification | Office | Project area |
|---|---|---|---|
| March 7, 2025 | Not classified | Philadelphia District Office |
Other documents for Teva Branded Pharmaceutical Products R&D, LLC
- FDA Inspection 1265377 - 2025-03-07
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