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FDA Inspection 1009805 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808000

The FDA completed an inspection of Sanofi Winthrop Industrie on March 3, 2017 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
March 3, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vitry-Sur-Seine (France)

Facility

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FDA data resources