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FDA Inspection 704478 — Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH — FEI 3003195501

The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on September 16, 2010 in Frankfurt Am Main. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 16, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frankfurt Am Main (Germany)

Facility

Other inspections at this facility

  • 1215824 (VAI Fri Mar 25 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1094836 (VAI Tue May 14 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1006001 (VAI Fri Mar 03 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952968 (NAI Thu Dec 10 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 933399 (VAI Fri Jun 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources