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FDA Inspection 1014635 — Fareva Amboise

Fareva Amboise — FEI 3000234005

The FDA completed an inspection of Fareva Amboise on May 16, 2017 in Poce Sur Cisse. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 16, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Poce Sur Cisse (France)

Facility

Other inspections at this facility

  • 1282366 (OAI Tue Sep 16 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1100819 (VAI Thu Dec 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1055251 (VAI Fri May 25 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 872367 (VAI Tue Mar 18 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 744219 (VAI Tue Sep 20 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources