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FDA Inspection 952968 — Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH — FEI 3003195501

The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on December 10, 2015 in Frankfurt Am Main. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
December 10, 2015
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Frankfurt Am Main (Germany)

Citations

IDCFRDescription
366921 CFR 820.20(c)Management review - defined interval, sufficient frequency

Facility

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  • 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))
  • 933399 (VAI Fri Jun 26 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 859523 (NAI Thu Dec 05 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources