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FDA Inspection 1020126 — Newport Medical Instruments Inc

Newport Medical Instruments Inc — FEI 2023050

The FDA completed an inspection of Newport Medical Instruments Inc on July 10, 2017 in Costa Mesa, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 10, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Costa Mesa, CA (United States)

Facility

Other inspections at this facility

  • 722370 (VAI Wed Apr 13 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 561409 (NAI Thu Jan 29 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources