FDA inspection
SEAGEN INC.: FDA inspection ending Jul 19, 2011
FDA inspection 742542 · Voluntary Action Indicated (VAI) · Bothell, WA
Key facts
| Inspection ID | 742542 |
|---|---|
| Firm | SEAGEN INC. |
| FEI number | 3002781621 |
| Address | 21717 30th Dr Se |
| City | Bothell |
| State | WA |
| ZIP | 98021 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Jul 19, 2011 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Bioresearch Monitoring |
| Product type | Drugs |
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