FDA Inspection 1056962 — Philips Respironics, Inc.
The FDA completed an inspection of Philips Respironics, Inc. on May 21, 2018 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
- May 21, 2018
- Fiscal Year
- 2018
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Murrysville, PA (United States)