FDA Inspection 1234784 — Carl Zeiss Meditec AG (Jena)

Carl Zeiss Meditec AG (Jena) — FEI 3001362763

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)