FDA inspection
Philips Ultrasound, Inc.: FDA inspection ending Jul 25, 2019
FDA inspection 1157003 · Voluntary Action Indicated (VAI) · Bothell, WA
Key facts
| Inspection ID | 1157003 |
|---|---|
| Firm | Philips Ultrasound, Inc. |
| FEI number | 3019216 |
| Address | 22100 Bothell Everett Hwy |
| City | Bothell |
| State | WA |
| ZIP | 98021-8431 |
| Fiscal year | 2019 |
| Inspection end date | Jul 25, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None 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