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FDA Inspection
•Taejoon Pharmaceutical Co., Ltd.•September 18, 2018

Taejoon Pharmaceutical Co., Ltd. – FDA Inspection, Sep 18, 2018

Record Details

This FDA Inspection record concerns Taejoon Pharmaceutical Co., Ltd., with an inspection on September 18, 2018, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Taejoon Pharmaceutical Co., Ltd.
Inspection Date
September 18, 2018
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Dennis Cantellops Paite (Issuing Officer)
  • Diane Goll (Issuing Officer)
View Company Profile

ID · 569c59be-c649-423f-a634-ee895f7102fc

Inspection Facts

Inspection number
1068405
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Taejoon Pharmaceutical Co., Ltd.

3
DateClassificationOfficeProject area
October 18, 2022VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 15, 2019OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 15, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Taejoon Pharmaceutical Co., Ltd.
  • FDA Inspection 1182340 - 2022-10-18
  • FDA Inspection 1106379 - 2019-10-15
  • FDA Inspection 994512 - 2016-11-15

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