FDA Inspection 1234249 — MASIMO CORPORATION

MASIMO CORPORATION — FEI 3013250653

The FDA completed an inspection of MASIMO CORPORATION on Mar 8, 2024 in Irvine, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 8, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Compliance: Devices
Location
Irvine, CA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.