# FDA Inspection 939905 - Dentis USA - August 27, 2015

Source: https://www.keypedia.com/records/fda_inspections/dentis-usa/cd3c3b57-47ca-40d5-a4e6-1a9c96bd7f6b
Source feed: FDA_Inspections

> FDA Inspection 939905 for Dentis USA on August 27, 2015. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 939905
- Company Name: Dentis USA
- Inspection Date: 2015-08-27
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 939905 - 2015-08-27](https://www.keypedia.com/records/fda_inspections/dentis-usa/9702e0d1-4609-4553-87e2-c5dc601afaa1)
- [FDA Inspection 939905 - 2015-08-27](https://www.keypedia.com/records/fda_inspections/dentis-usa/8af988a5-105d-440e-a2db-2a755be78db3)
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Company: https://www.keypedia.com/companies/dentis-usa/89973b0c-a9b2-4d8b-bf9e-da8fd27479cd

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