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FDA Inspection 1109449 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808000

The FDA completed an inspection of Sanofi Winthrop Industrie on September 13, 2019 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
September 13, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vitry-Sur-Seine (France)

Facility

Other inspections at this facility

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  • 1245906 (VAI Fri May 12 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1009805 (VAI Fri Mar 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 873415 (VAI Fri Mar 07 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 665406 (VAI Fri Apr 30 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources