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FDA Inspection
•Kindos Pharmaceuticals Co., Ltd.•July 19, 2024

Kindos Pharmaceuticals Co., Ltd. – FDA Inspection, Jul 19, 2024

Record Details

This FDA Inspection record concerns Kindos Pharmaceuticals Co., Ltd., with an inspection on July 19, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Kindos Pharmaceuticals Co., Ltd.
Inspection Date
July 19, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Michael A. Charles (FDA Associated Person)
View Company Profile

ID · 243d6f36-52b7-432b-841d-577271f5d963

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1244269
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Kindos Pharmaceuticals Co., Ltd.

5
DateClassificationOfficeProject area
July 30, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 1, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 2, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 10, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 24, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Kindos Pharmaceuticals Co., Ltd.
  • FDA Inspection 1101348 - 2019-07-30
  • FDA Inspection 1009271 - 2017-04-01
  • FDA Inspection 978257 - 2016-06-02
  • FDA Inspection 941452 - 2015-04-10
  • FDA Inspection 807892 - 2012-07-24

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