FDA Inspection 772774 — Catalent Germany Schorndorf GmbH
The FDA completed an inspection of Catalent Germany Schorndorf GmbH on Feb 10, 2012 in Schorndorf. 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
- Feb 10, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Schorndorf (Germany)