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FDA Inspection
•DentiMax , Inc•March 10, 2023

DentiMax , Inc – FDA Inspection, Mar 10, 2023

Record Details

This FDA Inspection record concerns DentiMax , Inc, with an inspection on March 10, 2023, issued by the Center for Devices and Radiological Health, covering devices.

Company
DentiMax , Inc
Inspection Date
March 10, 2023
Product Type
Devices
Office
Center for Devices and Radiological Health
Person
  • Charles L. Larson (Company Rep)
View Company Profile

ID · 5b6272be-5e17-4688-9310-a8c9f0b2e7dc

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1199964
FDA center
Medical Devices & Rad Health
Project area
Postmarket Assurance: Devices
Outcome
Form 483 issued

FDA Citations

2
  1. 21 CFR 820.198(e)Records of complaint investigation
  2. 21 CFR 820.50(a)(1)Documented evaluation

Full citation text and observation details available on the Dashboard.

Other FDA inspections of DentiMax , Inc

2
DateClassificationOfficeProject area
January 22, 2016VAICenter for Devices and Radiological HealthCompliance: Devices
April 22, 2011VAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for DentiMax , Inc
  • FDA Inspection 956623 - 2016-01-22
  • FDA Inspection 722016 - 2011-04-22

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