FDA Inspection 1301536 — Ethypharm

Ethypharm — FEI 3004715600

The FDA completed an inspection of Ethypharm on October 7, 2022 in Le Grand Quevilly CEDEX. 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
October 7, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Le Grand Quevilly CEDEX (France)

Additional Details

Mutual Recognition Agreement (MRA)