# DentiMax , Inc – FDA Inspection, Mar 10, 2023

Source: https://www.keypedia.com/records/fda_inspections/dentimax-inc/5b6272be-5e17-4688-9310-a8c9f0b2e7dc
Source feed: FDA_Inspections

> FDA inspection 1199964 of DentiMax , Inc, March 10, 2023. Classification: No Action Indicated (NAI). 2 citations under 21 CFR part 820. Form 483 issued. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1199964
- Company Name: DentiMax , Inc
- Inspection Date: 2023-03-10
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 956623 - 2016-01-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/dbc5a994-93ed-441f-8d9e-a69126139c82)
- [FDA Inspection 722016 - 2011-04-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/b49b48a9-d7b6-44f1-af58-55b7232e2f81)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/charles-l-larson/4232255d-bfd6-4616-a854-c801e4c23e1c)

Company: https://www.keypedia.com/companies/dentimax-inc/3bbeea11-6c03-4742-b6be-0d3f780b019f

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