FDA Inspection 1330948 — Klosterfrau Berlin GmbH

Klosterfrau Berlin GmbH — FEI 3004187716

The FDA completed an inspection of Klosterfrau Berlin GmbH on Oct 2, 2025 in Berlin. 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
Oct 2, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Berlin (Germany)

Additional Details

Mutual Recognition Agreement (MRA)