FDA inspection
WCG IRB, Inc: FDA inspection ending Sep 30, 2002
FDA inspection 239870 · No Action Indicated (NAI) · Puyallup, WA
Key facts
| Inspection ID | 239870 |
|---|---|
| Firm | WCG IRB, Inc |
| FEI number | 3021685 |
| Address | 1019 39th Ave Se Stes 120 And 205 |
| City | Puyallup |
| State | WA |
| ZIP | 98374-2118 |
| Fiscal year | 2002 |
| Inspection end date | Sep 30, 2002 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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