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FDA Inspection
•Zhejiang Tianyu Pharmaceutical Co. Ltd.•April 12, 2019

Zhejiang Tianyu Pharmaceutical Co. Ltd. – FDA Inspection, Apr 12, 2019

Record Details

This FDA Inspection record concerns Zhejiang Tianyu Pharmaceutical Co. Ltd., with an inspection on April 12, 2019, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Tianyu Pharmaceutical Co. Ltd.
Inspection Date
April 12, 2019
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Laurimer Kuilan-Torres (Issuing Officer)
View Company Profile

ID · a8ce6b2e-6711-4438-a756-07e69460d1a1

Inspection Facts

Official Action Indicated (OAI)

Significant objectionable conditions were found and regulatory or administrative action is recommended.

Inspection number
1086758
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Zhejiang Tianyu Pharmaceutical Co. Ltd.

3
DateClassificationOfficeProject area
November 29, 2024Not classifiedOffice of Inspections and Investigations
March 4, 2022OAICenter for Drug Evaluation and ResearchDrug Quality Assurance
June 12, 2015VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Tianyu Pharmaceutical Co. Ltd.
  • FDA Inspection 1258227 - 2024-11-29
  • FDA Inspection 1163904 - 2022-03-04
  • FDA Inspection 935989 - 2015-06-12

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