FDA Inspection 1253880 — SEAGEN INC.

SEAGEN INC. — FEI 3002781621

The FDA completed an inspection of SEAGEN INC. on November 1, 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
November 1, 2024
Fiscal Year
2025
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bothell, WA (United States)

Additional Details

Sponsor, Contract Research Organization