FDA inspection
SEAGEN INC.: FDA inspection ending Jan 5, 2018
FDA inspection 1040735 · No Action Indicated (NAI) · Bothell, WA
Key facts
| Inspection ID | 1040735 |
|---|---|
| Firm | SEAGEN INC. |
| FEI number | 3002781621 |
| Address | 21823 30th Dr Se |
| City | Bothell |
| State | WA |
| ZIP | 98021 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Jan 5, 2018 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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