FDA inspection
Welch Allyn Protocol, Inc: FDA inspection ending Aug 22, 2003
FDA inspection 288034 · Voluntary Action Indicated (VAI) · Beaverton, OR
Key facts
| Inspection ID | 288034 |
|---|---|
| Firm | Welch Allyn Protocol, Inc |
| FEI number | 3023750 |
| Address | 9525 SW Gemini Dr |
| City | Beaverton |
| State | OR |
| ZIP | 97008-7149 |
| Fiscal year | 2003 |
| Inspection end date | Aug 22, 2003 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med 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