# FDA Inspection 1010075 - Carl Zeiss Meditec AG - February 24, 2017

Source: https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-ag/3ee87128-d7fe-4bf9-b4aa-3c1112eee66c
Source feed: FDA_Inspections

> FDA Inspection 1010075 for Carl Zeiss Meditec AG on February 24, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1010075
- Company Name: Carl Zeiss Meditec AG
- Inspection Date: 2017-02-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 894790 - 2014-08-15](https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-ag/ae27253a-289a-4af2-b1fc-f3ed5258aa82)
- [FDA Inspection 894790 - 2014-08-15](https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-ag/a6a74481-9e97-403e-8059-6561fcf355d7)
- [FDA Inspection 894790 - 2014-08-15](https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-ag/61350f02-e20f-4739-a6f0-e328139e25a3)

Company: https://www.keypedia.com/companies/carl-zeiss-meditec-ag/8d514ab4-aabc-4309-9d8e-dbe3a0b44c77

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