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FDA Inspection
•Zhejiang Guobang Pharmaceutical Co., Ltd•March 3, 2025

Zhejiang Guobang Pharmaceutical Co., Ltd – FDA Inspection, Mar 3, 2025

Record Details

This FDA Inspection record concerns Zhejiang Guobang Pharmaceutical Co., Ltd, with an inspection on March 3, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Zhejiang Guobang Pharmaceutical Co., Ltd
Inspection Date
March 3, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Jose E. Almeida
  • Monica E. Murie (Investigator)
  • Victoria Spivak (FDA Associated Person)
View Company Profile

ID · 5b7338a2-d174-4e34-b992-4588896f6c96

Inspection Facts

Inspection number
1265595
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Zhejiang Guobang Pharmaceutical Co., Ltd

3
DateClassificationOfficeProject area
January 10, 2020VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
July 13, 2018Not classifiedOffice of Inspections and Investigations
September 24, 2015NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Guobang Pharmaceutical Co., Ltd
  • FDA Inspection 1134720 - 2020-01-10
  • FDA Inspection 1067561 - 2018-07-13
  • FDA Inspection 945403 - 2015-09-24

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