# FDA Inspection 967019 - Carl Zeiss Meditec USA, Inc. - March 25, 2016

Source: https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-usa-inc/12cdd7eb-3692-4ab2-be0e-1413e1288200
Source feed: FDA_Inspections

> FDA Inspection 967019 for Carl Zeiss Meditec USA, Inc. on March 25, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 967019
- Company Name: Carl Zeiss Meditec USA, Inc.
- Inspection Date: 2016-03-25
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/carl-zeiss-meditec-usa-inc/c825eb4a-ef11-4a95-bbdc-33f0a313cf55

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7