FDA Inspection
Sanofi Winthrop IndustrieSanofi Winthrop Industrie – FDA Inspection, Sep 29, 2017
Record Details
This FDA Inspection record concerns Sanofi Winthrop Industrie, with an inspection on September 29, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.
- Person
- MRA McCulloughJ (Issuing Officer)
View Company Profile
ID · 71b74f7d-a3e7-42a9-98d9-ffa48644add9
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1086424
- FDA center
- Human Drugs
- Project area
- Drug Quality Assurance
Other FDA inspections of Sanofi Winthrop Industrie
5| Date | Classification | Office | Project area |
|---|---|---|---|
| September 15, 2023 | Not classified | Office of Inspections and Investigations | |
| November 22, 2019 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| December 12, 2014 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| April 5, 2012 | NAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
| July 17, 2009 | VAI | Center for Drug Evaluation and Research | Drug Quality Assurance |
Other documents for Sanofi Winthrop Industrie
- FDA Inspection 1280258 - 2023-09-15
- FDA Inspection 1155911 - 2019-11-22
- FDA Inspection 909720 - 2014-12-12
- FDA Inspection 780612 - 2012-04-05
- FDA Inspection 602253 - 2009-07-17
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