FDA Inspection 1234784 — Carl Zeiss Meditec AG (Jena)
The FDA completed an inspection of Carl Zeiss Meditec AG (Jena) on Mar 7, 2024 in Jena. 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: Devices.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Mar 7, 2024
- Fiscal Year
- 2024
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Jena (Germany)