FDA Inspection 800990 — Umforana GmbH & Co. KG

Umforana GmbH & Co. KG — FEI 3003227179

The FDA completed an inspection of Umforana GmbH & Co. KG on Sep 13, 2012 in Wiesbaden. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 13, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wiesbaden (Germany)