FDA Inspection 1155911 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 1000476619

The FDA completed an inspection of Sanofi Winthrop Industrie on November 22, 2019 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
November 22, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Sisteron (France)

Additional Details

Mutual Recognition Agreement (MRA)