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FDA Inspection
•Shiratori Pharmaceutical Co. Ltd.•November 6, 2013

Shiratori Pharmaceutical Co. Ltd. – FDA Inspection, Nov 6, 2013

Record Details

This FDA Inspection record concerns Shiratori Pharmaceutical Co. Ltd., with an inspection on November 6, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shiratori Pharmaceutical Co. Ltd.
Inspection Date
November 6, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 658e61e0-acc5-454f-bbd4-f36fc209b9f2

Inspection Facts

Voluntary Action Indicated (VAI)

Objectionable conditions were found, but FDA is not prepared to take or recommend regulatory action.

Inspection number
855403
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Shiratori Pharmaceutical Co. Ltd.

2
DateClassificationOfficeProject area
October 18, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 4, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Shiratori Pharmaceutical Co. Ltd.
  • FDA Inspection 1109483 - 2019-10-18
  • FDA Inspection 994527 - 2016-11-04

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