FDA Inspection 1161948 — Gemini PharmChem Mannheim GmbH

Gemini PharmChem Mannheim GmbH — FEI 3014000756

The FDA completed an inspection of Gemini PharmChem Mannheim GmbH on Jan 21, 2022 in Mannheim. 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
Jan 21, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Mannheim (Germany)