FDA Inspection 1163825 — Rommelag CDMO Switzerland AG
The FDA completed an inspection of Rommelag CDMO Switzerland AG on Feb 11, 2022 in Zell Lu. 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
- Feb 11, 2022
- Fiscal Year
- 2022
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Zell Lu (Switzerland)