FDA Inspection 935340 — Rommelag CDMO Switzerland AG
The FDA completed an inspection of Rommelag CDMO Switzerland AG on Jul 3, 2015 in Zell Lu. 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
- Jul 3, 2015
- Fiscal Year
- 2015
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Zell Lu (Switzerland)