# FDA Inspection 1215652 - Dentlight Inc - August 23, 2023

Source: https://www.keypedia.com/records/fda_inspections/dentlight-inc/99d45cc7-7228-4de3-b4e0-9ba65576bded
Source feed: FDA_Inspections

> FDA Inspection 1215652 for Dentlight Inc on August 23, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1215652
- Company Name: Dentlight Inc
- Inspection Date: 2023-08-23
- 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 1215652 - 2023-08-23](https://www.keypedia.com/records/fda_inspections/dentlight-inc/c72d4782-0217-42cd-babf-0aa6f45c6786)
- [FDA Inspection 1062165 - 2018-08-15](https://www.keypedia.com/records/fda_inspections/dentlight-inc/252bd8ec-afef-4e3d-9491-d9094e3ba2d3)
- [FDA Inspection 661054 - 2010-04-26](https://www.keypedia.com/records/fda_inspections/dentlight-inc/ebef7daf-8615-4340-b9ca-518049a854c4)
- [FDA Inspection 661054 - 2010-04-26](https://www.keypedia.com/records/fda_inspections/dentlight-inc/04e17f75-8162-4c6d-9c91-7ff40234b7e5)

Company: https://www.keypedia.com/companies/dentlight-inc/545221f5-e0ed-408a-b31f-5927f5e686de

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