FDA Inspection
Sanofi Winthrop IndustrieSanofi Winthrop Industrie – FDA Inspection, Jul 13, 2018
Record Details
This FDA Inspection record concerns Sanofi Winthrop Industrie, with an inspection on July 13, 2018, issued by the Center for Biologics Evaluation and Research, covering biologics.
- People
- Arie Menachem (Issuing Officer)
- Xiaokuang Lai (FDA Associated Person)
View Company Profile
ID · 16482ad2-60b3-4aaf-9744-d4283b47bbaa
Inspection Facts
Voluntary Action Indicated (VAI)
Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.
- Inspection number
- 1059004
- FDA center
- Biologics
- Project area
- Blood and Blood Products
- Outcome
- Form 483 issued
Other FDA inspections of Sanofi Winthrop Industrie
4| Date | Classification | Office | Project area |
|---|---|---|---|
| January 26, 2024 | VAI | Center for Biologics Evaluation and Research | Vaccines and Allergenic Products |
| November 17, 2023 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| February 18, 2020 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
| July 28, 2016 | VAI | Center for Biologics Evaluation and Research | Blood and Blood Products |
Other documents for Sanofi Winthrop Industrie
- FDA Inspection 1227792 - 2024-01-26
- FDA Inspection 1223859 - 2023-11-17
- FDA Inspection 1120933 - 2020-02-18
- FDA Inspection 994790 - 2016-07-28
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