FDA Inspection 753733 — Carl Zeiss Meditec Inc.

Carl Zeiss Meditec Inc. — FEI 2918630

The FDA completed an inspection of Carl Zeiss Meditec Inc. on Nov 17, 2011 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
Nov 17, 2011
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Dublin, CA (United States)