FDA Inspection 1326638 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808000

The FDA completed an inspection of Sanofi Winthrop Industrie on October 4, 2024 in Vitry-Sur-Seine. 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
October 4, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vitry-Sur-Seine (France)

Additional Details

Mutual Recognition Agreement (MRA)