FDA Inspection 1236983 — SEAGEN INC.

SEAGEN INC. — FEI 3002781621

The FDA completed an inspection of SEAGEN INC. on May 2, 2024 in Bothell, WA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
May 2, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Bothell, WA (United States)