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Details of Daiwa Pharmaceuticals's U.S. FDA Inspections. Original Data: FDA Inspection Database

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01 Daiwa Pharmaceutical Co., Ltd. (1)

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01 Voluntary Action Indicated (1)

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01 2017-07-21 (1)

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01 Toyama (1)

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01 JP (1)

INSPECTIONS & REGISTRATIONS

URL Supplier Web Content
Voluntary Action Indicated
2017-07-21
Toyama
JP
ORA
CDER
Drug Quality Assurance
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