FDA Inspection 1208954 — Eurofins AmatsiGroup SAS

Eurofins AmatsiGroup SAS — FEI 3013529058

The FDA completed an inspection of Eurofins AmatsiGroup SAS on May 28, 2021 in Idron. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
May 28, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Idron (France)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.