FDA Inspection 1177330 — Umforana GmbH & Co. KG

Umforana GmbH & Co. KG — FEI 3003227179

The FDA completed an inspection of Umforana GmbH & Co. KG on Apr 12, 2022 in Wiesbaden. 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
Apr 12, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wiesbaden (Germany)

Additional Details

Mutual Recognition Agreement (MRA)