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FDA Inspection
•Guangzhou Hanpu Pharmaceutical Co. Ltd.•January 25, 2018

Guangzhou Hanpu Pharmaceutical Co. Ltd. – FDA Inspection, Jan 25, 2018

Record Details

This FDA Inspection record concerns Guangzhou Hanpu Pharmaceutical Co. Ltd., with an inspection on January 25, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Guangzhou Hanpu Pharmaceutical Co. Ltd.
Inspection Date
January 25, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Meisha R. Sampson (Issuing Officer)
View Company Profile

ID · d4994f8c-1692-4e93-8724-ee9e297c2f38

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1040600
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Guangzhou Hanpu Pharmaceutical Co. Ltd.

2
DateClassificationOfficeProject area
December 13, 2024Not classifiedOffice of Inspections and Investigations
July 19, 2013VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Guangzhou Hanpu Pharmaceutical Co. Ltd.
  • FDA Inspection 1259306 - 2024-12-13
  • FDA Inspection 844182 - 2013-07-19

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