FDA Inspection
Sanofi - Aventis US LLCSanofi - Aventis US LLC – FDA Inspection, Aug 18, 2010
Record Details
This FDA Inspection record concerns Sanofi - Aventis US LLC, with an inspection on August 18, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Company
- Sanofi - Aventis US LLC
- Inspection Date
- August 18, 2010
- Product Type
- Drugs
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ID · 9ecf07d9-3a2c-482d-8fdd-08be71ca693e
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 675841
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
FDA Citations
1- 21 CFR 211.111Deviations of production time limits
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Other FDA inspections of Sanofi - Aventis US LLC
2| Date | Classification | Office | Project area |
|---|---|---|---|
| December 12, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 27, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sanofi - Aventis US LLC
- FDA Inspection 906324 - 2014-12-12
- FDA Inspection 769605 - 2012-01-27
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