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FDA Inspection
•Tianjin Kingyork Pharmaceuticals Co., Ltd•July 5, 2013

Tianjin Kingyork Pharmaceuticals Co., Ltd – FDA Inspection, Jul 5, 2013

Record Details

This FDA Inspection record concerns Tianjin Kingyork Pharmaceuticals Co., Ltd, with an inspection on July 5, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Tianjin Kingyork Pharmaceuticals Co., Ltd
Inspection Date
July 5, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 54e834e6-6023-4989-b33a-715c0b0f8137

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
854753
FDA center
Human Drugs
Project area
Drug Quality Assurance

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
June 29, 2018Not classifiedOffice of Inspections and Investigations
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 1059208 - 2018-06-29

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