FDA Inspection 1326638 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808000

The FDA completed an inspection of Sanofi Winthrop Industrie on Oct 4, 2024 in Vitry-Sur-Seine. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Oct 4, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vitry-Sur-Seine (France)

Additional Details

Mutual Recognition Agreement (MRA)

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