# FDA Inspection 849198 - Coltene /Whaledent AG - September 19, 2013

Source: https://www.keypedia.com/records/fda_inspections/coltene-whaledent-ag/b35e810b-6210-4a1c-a321-da6eb7a55a44
Source feed: FDA_Inspections

> FDA Inspection 849198 for Coltene /Whaledent AG on September 19, 2013. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 849198
- Company Name: Coltene /Whaledent AG
- Inspection Date: 2013-09-19
- 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 849198 - 2013-09-19](https://www.keypedia.com/records/fda_inspections/coltene-whaledent-ag/e9ec6da1-2979-42b9-b18e-effac229dff1)
- [FDA Inspection 704248 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/coltene-whaledent-ag/1039f62d-d668-463c-83ca-2da0ada6fecb)
- [FDA Inspection 704248 - 2010-12-09](https://www.keypedia.com/records/fda_inspections/coltene-whaledent-ag/6ba035fd-18cf-4ad7-abda-021bbda335b0)

Company: https://www.keypedia.com/companies/coltene-whaledent-ag/2bc6b18d-ce8d-4302-a081-ae64499f6996

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