FDA Inspection 1117028 — Eurofins Amatsi Analytics

Eurofins Amatsi Analytics — FEI 3012886212

The FDA completed an inspection of Eurofins Amatsi Analytics on March 15, 2019 in Peyruis. 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 15, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Peyruis (France)

Additional Details

Mutual Recognition Agreement (MRA)