FDA Inspection 1124289 — Bioverativ USA Inc

Bioverativ USA Inc — FEI 3013359652

The FDA completed an inspection of Bioverativ USA Inc on Jun 23, 2020 in Bridgewater, NJ. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Jun 23, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Bridgewater, NJ (United States)

Additional details

Sponsor, Contract Research Organization

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