FDA Inspection 1141913 — Genmab US, Inc.

Genmab US, Inc. — FEI 3017003751

The FDA completed an inspection of Genmab US, Inc. on April 28, 2021 in Plainsboro, NJ. 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
April 28, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Plainsboro, NJ (United States)

Additional Details

Sponsor, Contract Research Organization