# FDA Inspection 894790 - Carl Zeiss Meditec AG - August 15, 2014

Source: https://www.keypedia.com/records/fda_inspections/carl-zeiss-meditec-ag/61350f02-e20f-4739-a6f0-e328139e25a3
Source feed: FDA_Inspections

> FDA Inspection 894790 for Carl Zeiss Meditec AG on August 15, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 894790
- Company Name: Carl Zeiss Meditec AG
- Inspection Date: 2014-08-15
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [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)

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