FDA Inspection 1103556 — Beigene USA, Inc.

Beigene USA, Inc. — FEI 3014478572

The FDA completed an inspection of Beigene USA, Inc. on September 13, 2019 in San Mateo, CA. 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
September 13, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
San Mateo, CA (United States)

Additional Details

Sponsor, Contract Research Organization