# FDA Inspection 956623 - DentiMax , Inc - January 22, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/dbc5a994-93ed-441f-8d9e-a69126139c82
Source feed: FDA_Inspections

> FDA Inspection 956623 for DentiMax , Inc on January 22, 2016. Classification: Voluntary Action Indicated (VAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 956623
- Company Name: DentiMax , Inc
- Inspection Date: 2016-01-22
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1199964 - 2023-03-10](https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/0ebf3e7e-ae49-4c6a-bb60-b28862b68baa)
- [FDA Inspection 1199964 - 2023-03-10](https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/5b6272be-5e17-4688-9310-a8c9f0b2e7dc)
- [FDA Inspection 956623 - 2016-01-22](https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/28737800-f060-4242-b8f8-6a8dad4530b9)
- [FDA Inspection 722016 - 2011-04-22](https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/16a19301-5c2f-44db-b46f-7a5fbe7912be)
- [FDA Inspection 722016 - 2011-04-22](https://www.globalkeysolutions.net/records/fda_inspections/dentimax-inc/b49b48a9-d7b6-44f1-af58-55b7232e2f81)

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

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