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FDA Inspection 1056962 — Philips Respironics, Inc.

Philips Respironics, Inc. — FEI 2518422

The FDA completed an inspection of Philips Respironics, Inc. on May 21, 2018 in Murrysville, PA. 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
May 21, 2018
Fiscal Year
2018
Product Type
Devices
Project Area
Compliance: Devices
Location
Murrysville, PA (United States)

Facility

Other inspections at this facility

  • 1170199 (VAI Thu May 19 2022 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1156266 (OAI Tue Nov 09 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1151497 (VAI Fri Sep 10 2021 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1114919 (OAI Fri Jan 10 2020 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 954800 (OAI Fri Jan 15 2016 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources