Home / Inspections / 1054784

FDA Inspection 1054784 — Fareva Mirabel

Fareva Mirabel — FEI 1000173162

The FDA completed an inspection of Fareva Mirabel on June 8, 2018 in Riom. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 8, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Riom (France)

Facility

Other inspections at this facility

  • 1271381 (VAI Fri Jul 22 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1124081 (VAI Fri Mar 15 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 955347 (VAI Tue Jan 19 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 885746 (VAI Thu May 22 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 732459 (VAI Mon May 23 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources