FDA Inspection 806113 — Excella GmbH & Co. KG
The FDA completed an inspection of Excella GmbH & Co. KG on Oct 10, 2012 in Feucht. 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 10, 2012
- Fiscal Year
- 2013
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Feucht (Germany)