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FDA Inspection
•Daiichi Sankyo Propharma Co., Ltd.•November 2, 2017

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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