FDA Inspection 1291084 — Eurofins PHAST GmbH

Eurofins PHAST GmbH — FEI 3005909718

The FDA completed an inspection of Eurofins PHAST GmbH on Dec 13, 2023 in Homburg. 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
Dec 13, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Homburg (Germany)

Additional Details

Mutual Recognition Agreement (MRA)