FDA Inspection 821445 — Recipharm Monts

Recipharm Monts — FEI 1000171152

The FDA completed an inspection of Recipharm Monts on February 26, 2013 in Monts. 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
February 26, 2013
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Monts (France)