FDA Inspection 1014497 — Daiichi Sankyo, Inc.

Daiichi Sankyo, Inc. — FEI 3003089536

The FDA completed an inspection of Daiichi Sankyo, Inc. on May 19, 2017 in Basking Ridge, 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
May 19, 2017
Fiscal Year
2017
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basking Ridge, NJ (United States)

Additional Details

Postmarket Adverse Drug Experience (PADE)