FDA Inspection 1335766 — Eurofins Amatsi Analytics

Eurofins Amatsi Analytics — FEI 3006118993

The FDA completed an inspection of Eurofins Amatsi Analytics on May 20, 2026 in Fontenilles. 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 20, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fontenilles (France)

Additional Details

Mutual Recognition Agreement (MRA)

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