FDA inspection
Philips North America LLC: FDA inspection ending Apr 24, 2013
FDA inspection 830352 · Voluntary Action Indicated (VAI) · Bothell, WA
Key facts
| Inspection ID | 830352 |
|---|---|
| Firm | Philips North America LLC |
| FEI number | 1000524572 |
| Address | 22100 Bothell Everett Hwy |
| City | Bothell |
| State | WA |
| ZIP | 98021 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Apr 24, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| 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