FDA inspection
WCG IRB, Inc: FDA inspection ending Nov 12, 2014
FDA inspection 908369 · Voluntary Action Indicated (VAI) · Puyallup, WA
Key facts
| Inspection ID | 908369 |
|---|---|
| Firm | WCG IRB, Inc |
| FEI number | 3021685 |
| Address | 1019 39th Ave Se Stes 120 And 205 |
| City | Puyallup |
| State | WA |
| ZIP | 98374 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Nov 12, 2014 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| 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