# Newport Medical Instruments Inc - Inspection Records

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

> Inspection records and compliance data for Newport Medical Instruments Inc in Costa Mesa, California. Access full analysis and detailed observations.

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## Details

- Name: Newport Medical Instruments Inc
- FEI Number: 2023050
- City: Costa Mesa
- State: California
- Country Name: United States
- Address Line 1: 1620 Sunflower Ave
- Zip Code: 92626

## Related Documents

- [FDA Inspection 1020126 - Newport Medical Instruments Inc - 2017-07-10](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/39fe4567-3803-4a81-b367-233786175c31) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2017
- [FDA Inspection 1020126 - Newport Medical Instruments Inc - 2017-07-10](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/aa0eaeae-0c06-4aaf-81be-a3dd0cf5e7ca) — classification: No Action Indicated (NAI), source: FDA, date: July 10, 2017
- [FDA Inspection 722370 - Newport Medical Instruments Inc - 2011-04-13](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/070eda2c-8686-4791-8be9-b910ff38b1a2) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2011
- [FDA Inspection 722370 - Newport Medical Instruments Inc - 2011-04-13](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/5a06becc-c20d-43ff-b492-cc793b3ba993) — classification: Voluntary Action Indicated (VAI), source: FDA, date: April 13, 2011
- [FDA Inspection 561409 - Newport Medical Instruments Inc - 2009-01-29](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/ef83b219-ad76-4339-8f03-c64bbf61ce4a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 29, 2009
- [FDA Inspection 561409 - Newport Medical Instruments Inc - 2009-01-29](https://www.keypedia.com/records/fda_inspections/newport-medical-instruments-inc/38e161e0-1f32-40da-b966-f205b47a0375) — classification: No Action Indicated (NAI), source: FDA, date: January 29, 2009

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