FDA Inspection 814715 — Ethypharm

Ethypharm — FEI 3002807933

The FDA completed an inspection of Ethypharm on September 13, 2012 in Chateauneuf En Thymerais. 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
September 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chateauneuf En Thymerais (France)