FDA Inspection
Sanofi-Aventis US LLCSanofi-Aventis US LLC – FDA Inspection, Jun 2, 2017
Record Details
This FDA Inspection record concerns Sanofi-Aventis US LLC, with an inspection on June 2, 2017, issued by the Kansas City District Office, covering animal drugs & feeds.
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ID · f4df2dd4-42e3-4775-8cb8-663c6037be96
Inspection Facts
- Inspection number
- 1012790
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
- Outcome
- Form 483 issued
FDA Citations
2- 21 CFR 211.192Extent of discrepancy, failure investigations
- 21 CFR 211.22(d)Procedures not in writing, fully followed
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Other FDA inspections of Sanofi-Aventis US LLC
4| Date | Classification | Office | Project area |
|---|---|---|---|
| February 12, 2014 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 14, 2012 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| October 6, 2010 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| January 28, 2009 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sanofi-Aventis US LLC
- FDA Inspection 867881 - 2014-02-12
- FDA Inspection 772113 - 2012-03-14
- FDA Inspection 684201 - 2010-10-06
- FDA Inspection 563141 - 2009-01-28
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