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FDA Inspection 1063584 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808341

The FDA completed an inspection of Sanofi Winthrop Industrie on July 17, 2018 in Aramon. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Biologics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 17, 2018
Fiscal Year
2018
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aramon (France)

Facility

Other inspections at this facility

  • 1246180 (VAI Fri Mar 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1118089 (VAI Fri Mar 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022342 (VAI Tue Jul 25 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998080 (VAI Wed Sep 14 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 857683 (NAI Fri Oct 25 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources