FDA Inspection 975602 — Minakem Dunkerque Production

Minakem Dunkerque Production — FEI 3008093605

The FDA completed an inspection of Minakem Dunkerque Production on April 22, 2016 in Dunkirk. 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
April 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Dunkirk (France)