FDA Inspection 1242229 — Carl Zeiss Meditec Inc.

Carl Zeiss Meditec Inc. — FEI 2918630

The FDA completed an inspection of Carl Zeiss Meditec Inc. on Mar 26, 2024 in Dublin, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 26, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Dublin, CA (United States)

Additional Details

Sponsor, Contract Research Organization