FDA Inspection 801960 — Patheon Softgels Inc
The FDA completed an inspection of Patheon Softgels Inc on Sep 26, 2012 in High Point, NC. 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
- Sep 26, 2012
- Fiscal Year
- 2012
- Product Type
- Drugs
- Project Area
- Bioresearch Monitoring
- Location
- High Point, NC (United States)
Additional Details
Postmarket Adverse Drug Experience (PADE)