# Newport Medical Instruments Inc – FDA Inspection, Jul 10, 2017

Source: https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/aa0eaeae-0c06-4aaf-81be-a3dd0cf5e7ca
Source feed: FDA_Inspections

> FDA inspection 1020126 of Newport Medical Instruments Inc, July 10, 2017. Classification: No Action Indicated (NAI). 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1020126
- Company Name: Newport Medical Instruments Inc
- Inspection Date: 2017-07-10
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- [FDA Inspection 722370 - 2011-04-13](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/5a06becc-c20d-43ff-b492-cc793b3ba993)
- FDA Inspection 561409 - 2009-01-29

## Related Officers

- [FDA Associated Person](https://www.keypedia.com/people/leonard-h-lavi/afe5082f-67e5-4bf2-a981-022756e93eb4)

Company: https://www.keypedia.com/companies/newport-medical-instruments-inc/b0da0add-2eb9-402e-bef6-3ef78392d3de

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