FDA inspection
Philips Respironics, Inc.: FDA inspection ending Nov 9, 2021
FDA inspection 1156266 · Official Action Indicated (OAI) · Murrysville, PA
Key facts
| Inspection ID | 1156266 |
|---|---|
| Firm | Philips Respironics, Inc. |
| FEI number | 2518422 |
| Address | 1001 Murry Ridge Ln |
| City | Murrysville |
| State | PA |
| ZIP | 15668 |
| Country | United States |
| Fiscal year | 2022 |
| Inspection end date | Nov 9, 2021 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data