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FDA Inspection 1073302 — Philips North America LLC

Philips North America LLC — FEI 1000524572

The FDA completed an inspection of Philips North America LLC on December 3, 2018 in Bothell, WA. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
December 3, 2018
Fiscal Year
2019
Product Type
Devices
Project Area
Compliance: Devices
Location
Bothell, WA (United States)

Facility

Other inspections at this facility

  • 1182153 (VAI Thu Oct 27 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1149323 (VAI Fri Aug 20 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1121760 (NAI Wed Mar 25 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 923916 (OAI Tue Apr 21 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 830352 (VAI Wed Apr 24 2013 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources