FDA Inspection 1332538 — Ricola Ag
The FDA completed an inspection of Ricola Ag on Feb 9, 2024 in Laufen. 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 9, 2024
- Fiscal Year
- 2024
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Laufen (Switzerland)
Additional Details
Mutual Recognition Agreement (MRA)