FDA Inspection
Sanofi-Aventis Deutschland GmbHSanofi-Aventis Deutschland GmbH – FDA Inspection, Sep 16, 2010
Record Details
This FDA Inspection record concerns Sanofi-Aventis Deutschland GmbH, with an inspection on September 16, 2010, issued by the Center for Drug Evaluation and Research, covering drugs.
- Inspection Date
- September 16, 2010
- Product Type
- Drugs
View Company Profile
ID · 40940da5-e64b-436b-bf23-9cba44c1366a
Inspection Facts
Official Action Indicated (OAI)
Significant objectionable conditions were found and regulatory or administrative action is recommended.
- Inspection number
- 704478
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Sanofi-Aventis Deutschland GmbH
11| Date | Classification | Office | Project area |
|---|---|---|---|
| January 16, 2025 | Not classified | Office of Inspections and Investigations | |
| March 25, 2022 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| May 14, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| March 3, 2017 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 10, 2015 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Sanofi-Aventis Deutschland GmbH
- FDA Inspection 1262770 - 2025-01-16
- FDA Inspection 1215824 - 2022-03-25
- FDA Inspection 1094836 - 2019-05-14
- FDA Inspection 1006001 - 2017-03-03
- FDA Inspection 952968 - 2015-12-10
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