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FDA Inspection
•Nomir Medical Technologies•July 17, 2015

Nomir Medical Technologies – FDA Inspection, Jul 17, 2015

Record Details

This FDA Inspection record concerns Nomir Medical Technologies, with an inspection on July 17, 2015, issued by the Center for Devices and Radiological Health, covering devices.

Company
Nomir Medical Technologies
Inspection Date
July 17, 2015
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 9f775022-5921-4a7c-b653-2926d1b15f60

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
935381
FDA center
Medical Devices & Rad Health
Project area
Radiation Control and Health Safety Act

FDA Citations

2
  1. 21 CFR 820.22Quality Audit/Reaudit - conducted
  2. 21 CFR 820.186QSR

Full citation text and observation details available on the Dashboard.

Other FDA inspections of Nomir Medical Technologies

2
DateClassificationOfficeProject area
May 24, 2013NAICenter for Devices and Radiological HealthCompliance: Devices
January 20, 2012NAICenter for Devices and Radiological HealthRadiation Control and Health Safety Act
Other documents for Nomir Medical Technologies
  • FDA Inspection 835298 - 2013-05-24
  • FDA Inspection 764082 - 2012-01-20

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