FDA Inspection 922940 — Eisai, Inc.

Eisai, Inc. — FEI 3009413786

The FDA completed an inspection of Eisai, Inc. on Apr 20, 2015 in Nutley, 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
Apr 20, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Nutley, NJ (United States)

Additional details

Postmarket Adverse Drug Experience (PADE)

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