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FDA Inspection 998080 — Sanofi Winthrop Industrie

Sanofi Winthrop Industrie — FEI 3002808341

The FDA completed an inspection of Sanofi Winthrop Industrie on September 14, 2016 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
September 14, 2016
Fiscal Year
2016
Product Type
Biologics
Project Area
Blood and Blood Products
Location
Aramon (France)

Facility

Other inspections at this facility

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  • 1118089 (VAI Fri Mar 29 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1063584 (VAI Tue Jul 17 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1022342 (VAI Tue Jul 25 2017 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