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FDA Inspection
•Daito Pharmaceutical Co., Ltd.•November 10, 2017

Daito Pharmaceutical Co., Ltd. – FDA Inspection, Nov 10, 2017

Record Details

This FDA Inspection record concerns Daito Pharmaceutical Co., Ltd., with an inspection on November 10, 2017, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Daito Pharmaceutical Co., Ltd.
Inspection Date
November 10, 2017
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Arsen Karapetyan
View Company Profile

ID · b2ca8f6e-e975-4d14-96d8-5a032a43ddd6

Inspection Facts

Inspection number
1037107
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Daito Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
December 19, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 16, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 29, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Daito Pharmaceutical Co., Ltd.
  • FDA Inspection 1226666 - 2023-12-19
  • FDA Inspection 1180850 - 2022-09-16
  • FDA Inspection 748400 - 2011-09-29

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