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FDA Inspection
•Tianjin Kingyork Pharmaceuticals Co., Ltd•June 29, 2018

Tianjin Kingyork Pharmaceuticals Co., Ltd – FDA Inspection, Jun 29, 2018

Record Details

This FDA Inspection record concerns Tianjin Kingyork Pharmaceuticals Co., Ltd, with an inspection on June 29, 2018, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Tianjin Kingyork Pharmaceuticals Co., Ltd
Inspection Date
June 29, 2018
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Chaoying C. Ma (Issuing Officer)
  • Joel D. Hustedt (FDA Associated Person)
View Company Profile

ID · f67d59fa-4a6e-4dcd-9405-87f0c300f098

Inspection Facts

Inspection number
1059208
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Tianjin Kingyork Pharmaceuticals Co., Ltd

6
DateClassificationOfficeProject area
July 31, 2026Not classifiedOffice of Inspections and InvestigationsDrug Quality Assurance
July 26, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 27, 2019Not classifiedOffice of Inspections and Investigations
May 31, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 1, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
View all 6 other inspections on the company page
Other documents for Tianjin Kingyork Pharmaceuticals Co., Ltd
  • FDA Inspection 1331476 - 2026-07-31
  • FDA Inspection 1246994 - 2024-07-26
  • FDA Inspection 1102217 - 2019-08-27
  • FDA Inspection 1095299 - 2019-05-31
  • FDA Inspection 986374 - 2016-09-01

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