FDA Inspection 1277224 - Daiichi Sankyo, Inc. - August 01, 2025

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Record Details

This FDA Inspection record concerns Daiichi Sankyo, Inc., with an inspection on August 1, 2025, issued by the New Jersey District Office, covering human drugs.

Company: Daiichi Sankyo, Inc.
Inspection Date: August 1, 2025
Product Type: Human Drugs
Office: New Jersey District Office

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ID · 63bf611c-4ad7-4991-8f19-7cdec7f9e84b

Violation Codes2

FD&C Act 505-1(f)(3)(A)FD&C Act 505-1(f)(4)

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