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FDA Inspection
•Carl Zeiss Meditec USA, Inc.•March 26, 2014

Carl Zeiss Meditec USA, Inc. – FDA Inspection, Mar 26, 2014

Record Details

This FDA Inspection record concerns Carl Zeiss Meditec USA, Inc., with an inspection on March 26, 2014, issued by the Center for Devices and Radiological Health, covering devices.

Company
Carl Zeiss Meditec USA, Inc.
Inspection Date
March 26, 2014
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · bd15360c-f118-40f4-84b9-8b6a7158352c

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
871600
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices

Other FDA inspections of Carl Zeiss Meditec USA, Inc.

6
DateClassificationOfficeProject area
March 26, 2024NAICenter for Devices and Radiological HealthBioresearch Monitoring
October 25, 2018NAICenter for Devices and Radiological HealthCompliance: Devices
March 25, 2016NAICenter for Devices and Radiological HealthCompliance: Devices
September 18, 2014NAICenter for Devices and Radiological HealthBioresearch Monitoring
November 17, 2011NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
View all 6 other inspections on the company page
Other documents for Carl Zeiss Meditec USA, Inc.
  • FDA Inspection 1242229 - 2024-03-26
  • FDA Inspection 1071053 - 2018-10-25
  • FDA Inspection 967019 - 2016-03-25
  • FDA Inspection 896573 - 2014-09-18
  • FDA Inspection 753733 - 2011-11-17

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