FDA Inspection 1032011 - Daiichi Sankyo Propharma Co., Ltd. - November 02, 2017

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Record Details

This FDA Inspection record concerns Daiichi Sankyo Propharma Co., Ltd., with an inspection on November 2, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company: Daiichi Sankyo Propharma Co., Ltd.
Inspection Date: November 2, 2017
Product Type: Drugs
Office: Center for Drug Evaluation and Research

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ID · 9070c8d4-53c7-4b95-bbd3-84d004ef030b

Violation Codes3

21 CFR 211.160(a)21 CFR 211.19221 CFR 211.22(d)

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