FDA Inspection 1231135 — EUROAPI Germany GmbH

EUROAPI Germany GmbH — FEI 3020754015

The FDA completed an inspection of EUROAPI Germany GmbH on Mar 4, 2022 in Frankfurt Am Main. 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
Mar 4, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frankfurt Am Main (Germany)

Additional Details

Mutual Recognition Agreement (MRA)