# FDA Inspection 1064729 - Dentium USA - August 10, 2018

Source: https://www.keypedia.com/records/fda_inspections/dentium-usa/4110dd6f-0d85-4df9-a46a-fb10c3e9cf79
Source feed: FDA_Inspections

> FDA Inspection 1064729 for Dentium USA on August 10, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1064729
- Company Name: Dentium USA
- Inspection Date: 2018-08-10
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/dentium-usa/fc202852-f833-4726-887d-35d3af9af1ef

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