# Nomir Medical Technologies – FDA Inspection, Jul 17, 2015

Source: https://www.keypedia.com/records/fda_inspections/nomir-medical-technologies/9f775022-5921-4a7c-b653-2926d1b15f60
Source feed: FDA_Inspections

> FDA inspection 935381 of Nomir Medical Technologies, July 17, 2015. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 935381
- Company Name: Nomir Medical Technologies
- Inspection Date: 2015-07-17
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 835298 - 2013-05-24](https://www.keypedia.com/records/fda_inspections/nomir-medical-technologies/d2862453-c089-4dbf-9975-22bf959278f4)
- [FDA Inspection 764082 - 2012-01-20](https://www.keypedia.com/records/fda_inspections/nomir-medical-technologies/d6691b61-0bd4-45b8-b182-087616e78b81)

Company: https://www.keypedia.com/companies/nomir-medical-technologies/d569055e-27b8-49a1-8249-451590285891

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