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FDA Inspection
•Zhejiang Langhua Pharmaceutical Co. Ltd.•November 21, 2014

Zhejiang Langhua Pharmaceutical Co. Ltd. – FDA Inspection, Nov 21, 2014

Record Details

This FDA Inspection record concerns Zhejiang Langhua Pharmaceutical Co. Ltd., with an inspection on November 21, 2014, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Langhua Pharmaceutical Co. Ltd.
Inspection Date
November 21, 2014
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · ffd85d4b-d8db-46e2-abfc-b8bd1f074dbb

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
906650
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Langhua Pharmaceutical Co. Ltd.

3
DateClassificationOfficeProject area
August 30, 2024VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
March 23, 2018NAICenter 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 1250797 - 2024-08-30
  • FDA Inspection 1049002 - 2018-03-23
  • FDA Inspection 774858 - 2012-03-01

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