FDA Inspection 1119141 — SEAGEN INC.

SEAGEN INC. — FEI 3002781621

The FDA completed an inspection of SEAGEN INC. on Jan 24, 2020 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Jan 24, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bothell, WA (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.