FDA Inspection
Carl Zeiss Meditec USA, Inc.Carl Zeiss Meditec USA, Inc. – FDA Inspection, Oct 25, 2018
Record Details
This FDA Inspection record concerns Carl Zeiss Meditec USA, Inc., with an inspection on October 25, 2018, issued by the Center for Devices and Radiological Health, covering devices.
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ID · d93e1d57-1b52-4a1e-ab53-ab259ccb48e0
Inspection Facts
No Action Indicated (NAI)
No objectionable conditions or practices were found during the inspection.
- Inspection number
- 1071053
- FDA center
- Medical Devices & Rad Health
- Project area
- Compliance: Devices
Other FDA inspections of Carl Zeiss Meditec USA, Inc.
6| Date | Classification | Office | Project area |
|---|---|---|---|
| March 26, 2024 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 25, 2016 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| September 18, 2014 | NAI | Center for Devices and Radiological Health | Bioresearch Monitoring |
| March 26, 2014 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
| November 17, 2011 | NAI | Center for Devices and Radiological Health | Postmarket Assurance: Devices |
Other documents for Carl Zeiss Meditec USA, Inc.
- FDA Inspection 1242229 - 2024-03-26
- FDA Inspection 967019 - 2016-03-25
- FDA Inspection 896573 - 2014-09-18
- FDA Inspection 871600 - 2014-03-26
- FDA Inspection 753733 - 2011-11-17
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