# DentiMax , Inc - Inspection Records

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

> Inspection records and compliance data for DentiMax , Inc in Mesa, Arizona. Access full analysis and detailed observations.

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## Details

- Name: DentiMax , Inc
- FEI Number: 3007515144
- City: Mesa
- State: Arizona
- Country Name: United States
- Address Line 1: 4115 E Valley Auto Dr Ste 101
- Zip Code: 85206

## Related Documents

- [483 - DentiMax , Inc - 2023-03-10](https://www.keypedia.com/records/483/dentimax-inc/823375d2-7cb6-43e4-aad3-8a3ee3df5f65) — source: FDA, date: March 10, 2023
- [FDA Inspection 1199964 - DentiMax , Inc - 2023-03-10](https://www.keypedia.com/records/fda_inspections/dentimax-inc/0ebf3e7e-ae49-4c6a-bb60-b28862b68baa) — classification: Voluntary Action Indicated (VAI), source: FDA, date: March 10, 2023
- [FDA Inspection 1199964 - DentiMax , Inc - 2023-03-10](https://www.keypedia.com/records/fda_inspections/dentimax-inc/5b6272be-5e17-4688-9310-a8c9f0b2e7dc) — classification: No Action Indicated (NAI), source: FDA, date: March 10, 2023
- [FDA Inspection 956623 - DentiMax , Inc - 2016-01-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/dbc5a994-93ed-441f-8d9e-a69126139c82) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2016
- [FDA Inspection 956623 - DentiMax , Inc - 2016-01-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/28737800-f060-4242-b8f8-6a8dad4530b9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 22, 2016
- [FDA Inspection 722016 - DentiMax , Inc - 2011-04-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/16a19301-5c2f-44db-b46f-7a5fbe7912be) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 22, 2011
- [FDA Inspection 722016 - DentiMax , Inc - 2011-04-22](https://www.keypedia.com/records/fda_inspections/dentimax-inc/b49b48a9-d7b6-44f1-af58-55b7232e2f81) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 22, 2011

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