# Newport Medical Instruments Inc – FDA Inspection, Apr 13, 2011

Source: https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/5a06becc-c20d-43ff-b492-cc793b3ba993
Source feed: FDA_Inspections

> FDA inspection 722370 of Newport Medical Instruments Inc, April 13, 2011. Classification: Voluntary Action Indicated (VAI). 10 citations under 21 CFR parts 803, 806 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 722370
- Company Name: Newport Medical Instruments Inc
- Inspection Date: 2011-04-13
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 10

## Related Documents

- [FDA Inspection 1020126 - 2017-07-10](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/aa0eaeae-0c06-4aaf-81be-a3dd0cf5e7ca)
- FDA Inspection 561409 - 2009-01-29

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