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FDA Inspection
•Zhejiang Tiantai Pharmaceutical Co., Ltd.•May 24, 2024

Zhejiang Tiantai Pharmaceutical Co., Ltd. – FDA Inspection, May 24, 2024

Record Details

This FDA Inspection record concerns Zhejiang Tiantai Pharmaceutical Co., Ltd., with an inspection on May 24, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Tiantai Pharmaceutical Co., Ltd.
Inspection Date
May 24, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Rowena S. Nguyen (Issuing Officer)
View Company Profile

ID · 61204884-b283-45b7-8d9e-07823088dbab

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1242708
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Tiantai Pharmaceutical Co., Ltd.

2
DateClassificationOfficeProject area
March 24, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 25, 2013NAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
Other documents for Zhejiang Tiantai Pharmaceutical Co., Ltd.
  • FDA Inspection 972159 - 2016-03-24
  • FDA Inspection 880979 - 2013-10-25

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