FDA Inspection 1307164 — argenx BV

argenx BV — FEI 3020999966

The FDA completed an inspection of argenx BV on March 6, 2026 in Boston, MA. 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
March 6, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Boston, MA (United States)

Additional Details

Sponsor, Contract Research Organization