FDA Inspection 576014 — Arevipharma GmbH
The FDA completed an inspection of Arevipharma GmbH on Apr 8, 2009 in Radebeul. 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: Veterinary.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Apr 8, 2009
- Fiscal Year
- 2009
- Product Type
- Veterinary
- Project Area
- Pre-Approval Eval. of Animal Drugs and Food Additives
- Location
- Radebeul (Germany)