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FDA Inspection 1011370 — Masimo Corporation

Masimo Corporation — FEI 3001452206

The FDA completed an inspection of Masimo Corporation on May 5, 2017 in Irvine, 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
May 5, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Irvine, CA (United States)

Facility

Other inspections at this facility

  • 1067514 (NAI Thu Sep 13 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 851391 (OAI Thu Oct 03 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 711962 (NAI Fri Feb 11 2011 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 649261 (NAI Wed Feb 03 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources