FDA Inspection 1240850 — Eurofins Pharma Quality Control

Eurofins Pharma Quality Control — FEI 3010164760

The FDA completed an inspection of Eurofins Pharma Quality Control on March 17, 2022 in Les Ulis. 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
March 17, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Les Ulis (France)

Additional Details

Mutual Recognition Agreement (MRA)