FDA inspection
Philips Electronics North America Corporation: FDA inspection ending Aug 31, 2017
FDA inspection 1023742 · Voluntary Action Indicated (VAI) · Saint Louis, MO
Key facts
| Inspection ID | 1023742 |
|---|---|
| Firm | Philips Electronics North America Corporation |
| FEI number | 1937850 |
| Address | 2039 Concourse Dr |
| City | Saint Louis |
| State | MO |
| ZIP | 63146 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Aug 31, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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
- 1–9 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