# FDA Inspection 909439 - Inkutec Gmbh - December 04, 2014

Source: https://www.keypedia.com/records/fda_inspections/inkutec-gmbh/83f48e4d-b025-42cb-bde2-2a6d31672d2d
Source feed: FDA_Inspections

> FDA Inspection 909439 for Inkutec Gmbh on December 04, 2014. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 909439
- Company Name: Inkutec Gmbh
- Inspection Date: 2014-12-04
- 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 909439 - 2014-12-04](https://www.keypedia.com/records/fda_inspections/inkutec-gmbh/f17cb89a-ed20-4fad-a885-3031fb827948)

Company: https://www.keypedia.com/companies/inkutec-gmbh/4d1b2f13-0835-4fc7-ace0-12cd1300e1f4

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