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FDA Inspection
•Yung Shin Pharmaceutical Industry Co., Ltd.•August 7, 2026

Yung Shin Pharmaceutical Industry Co., Ltd. – FDA Inspection, Aug 7, 2026

Record Details

This FDA Inspection record concerns Yung Shin Pharmaceutical Industry Co., Ltd., with an inspection on August 7, 2026, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Yung Shin Pharmaceutical Industry Co., Ltd.
Inspection Date
August 7, 2026
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Jolanna A. Norton (FDA Associated Person)
View Company Profile

ID · 9a419997-58b6-4fd3-9946-e9e8e170152d

Inspection Facts

Inspection number
1338914
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Yung Shin Pharmaceutical Industry Co., Ltd.

9
DateClassificationOfficeProject area
April 25, 2024Not classifiedOffice of Inspections and Investigations
October 22, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 12, 2019VAIOffice of Inspections and InvestigationsGeneric Drug Evaluation
July 27, 2018VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 24, 2016Not classifiedOffice of Inspections and Investigations
View all 9 other inspections on the company page
Other documents for Yung Shin Pharmaceutical Industry Co., Ltd.
  • FDA Inspection 1238384 - 2024-04-25
  • FDA Inspection 1111111 - 2019-10-22
  • FDA Inspection 1101829 - 2019-09-12
  • FDA Inspection 1062411 - 2018-07-27
  • FDA Inspection 997026 - 2016-11-24

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