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FDA Inspection
•Zhejiang Langhua Pharmaceutical Co. Ltd.•August 30, 2024

Zhejiang Langhua Pharmaceutical Co. Ltd. – FDA Inspection, Aug 30, 2024

Record Details

This FDA Inspection record concerns Zhejiang Langhua Pharmaceutical Co. Ltd., with an inspection on August 30, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Langhua Pharmaceutical Co. Ltd.
Inspection Date
August 30, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Alan A. Rivera
  • Chad W. Rice (Company Rep)
View Company Profile

ID · b21ab25a-1b58-4d2a-b235-eee5dd933e10

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1250797
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Langhua Pharmaceutical Co. Ltd.

3
DateClassificationOfficeProject area
March 23, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
November 21, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 1, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Langhua Pharmaceutical Co. Ltd.
  • FDA Inspection 1049002 - 2018-03-23
  • FDA Inspection 906650 - 2014-11-21
  • FDA Inspection 774858 - 2012-03-01

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