FDA Inspection 1051401 — Carl Zeiss Meditec AG (Jena)

Carl Zeiss Meditec AG (Jena) — FEI 3001362763

The FDA completed an inspection of Carl Zeiss Meditec AG (Jena) on Apr 26, 2018 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). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Apr 26, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Radiation Control and Health Safety Act
Location
Jena (Germany)

Citations

IDCFRDescription
369621 CFR 820.100(b)Documentation