FDA Inspection 1318108 — Daiichi Sankyo, Inc.

Daiichi Sankyo, Inc. — FEI 3003089536

The FDA completed an inspection of Daiichi Sankyo, Inc. on May 4, 2026 in Basking Ridge, NJ. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
May 4, 2026
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Basking Ridge, NJ (United States)

Additional Details

Sponsor, Contract Research Organization

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