# FDA Inspection 908473 - ALTATEC GmbH - December 08, 2014

Source: https://www.keypedia.com/records/fda_inspections/altatec-gmbh/09d03e36-baee-4b43-893e-6a591b0ecf6d
Source feed: FDA_Inspections

> FDA Inspection 908473 for ALTATEC GmbH on December 08, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 908473
- Company Name: ALTATEC GmbH
- Inspection Date: 2014-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 908473 - 2014-12-08](https://www.keypedia.com/records/fda_inspections/altatec-gmbh/074a8a79-f25d-4502-abf1-5c8943eba154)

Company: https://www.keypedia.com/companies/altatec-gmbh/4aca2a39-71fd-4f1f-8307-5930356eae11

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