FDA Inspection 862778 — Finorga

Finorga — FEI 3002806998

The FDA completed an inspection of Finorga on December 13, 2013 in Mourenx. 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
December 13, 2013
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mourenx (France)