FDA Inspection 586472 — Patheon Austria GmbH & Co. KG
The FDA completed an inspection of Patheon Austria GmbH & Co. KG on May 8, 2009 in Linz. 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
- May 8, 2009
- Fiscal Year
- 2009
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Linz (Austria)