# FDA Inspection 949302 - Anaxdent North America LLC - November 19, 2015

Source: https://www.globalkeysolutions.net/records/fda_inspections/anaxdent-north-america-llc/de808785-84dc-46d4-a39d-1241b63ee17e
Source feed: FDA_Inspections

> FDA Inspection 949302 for Anaxdent North America LLC on November 19, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 949302
- Company Name: Anaxdent North America LLC
- Inspection Date: 2015-11-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 949302 - 2015-11-19](https://www.globalkeysolutions.net/records/fda_inspections/anaxdent-north-america-llc/41686c36-add1-4c52-90f5-7359ce935418)

Company: https://www.globalkeysolutions.net/companies/anaxdent-north-america-llc/3230227a-bb7d-4383-ab82-14acc14ef6f7

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