FDA Inspection 909720 — Sanofi Winthrop Industrie
The FDA completed an inspection of Sanofi Winthrop Industrie on December 12, 2014 in Sisteron. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 12, 2014
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sisteron (France)