FDA Inspection 1085912 — Ethypharm

Ethypharm — FEI 3002807933

The FDA completed an inspection of Ethypharm on February 22, 2018 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
February 22, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chateauneuf En Thymerais (France)

Additional Details

Mutual Recognition Agreement (MRA)