FDA Inspection 954800 — Philips Respironics, Inc.
The FDA completed an inspection of Philips Respironics, Inc. on Jan 15, 2016 in Murrysville, PA. The inspection was classified OAI (Official Action Indicated — regulatory and/or administrative actions are recommended). Product area: Devices.
Inspection Details
- Classification
- Official Action Indicated (OAI)
- End Date
- Jan 15, 2016
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Murrysville, PA (United States)