FDA Inspection 654570 — Catalent Germany Eberbach GmbH
The FDA completed an inspection of Catalent Germany Eberbach GmbH on Mar 5, 2010 in Eberbach. 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
- Mar 5, 2010
- Fiscal Year
- 2010
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Eberbach (Germany)