FDA Inspection 1124081 — Fareva Mirabel

Fareva Mirabel — FEI 1000173162

The FDA completed an inspection of Fareva Mirabel on March 15, 2019 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
March 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Riom (France)

Additional Details

Mutual Recognition Agreement (MRA)