FDA Inspection 675886 — Daiichi Sankyo, Inc.

Daiichi Sankyo, Inc. — FEI 3003089536

The FDA completed an inspection of Daiichi Sankyo, Inc. on Aug 12, 2010 in Basking Ridge, 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
Aug 12, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basking Ridge, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)

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