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FDA Inspection
•Zhejiang Excel Pharmaceutical Company, Ltd.•April 12, 2024

Zhejiang Excel Pharmaceutical Company, Ltd. – FDA Inspection, Apr 12, 2024

Record Details

This FDA Inspection record concerns Zhejiang Excel Pharmaceutical Company, Ltd., with an inspection on April 12, 2024, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Excel Pharmaceutical Company, Ltd.
Inspection Date
April 12, 2024
Product Type
Drugs
Office
Center for Drug Evaluation and Research
People
  • Damaris Y. Hernandez (Investigator)
  • Suzanne N. Vallez (FDA Associated Person)
View Company Profile

ID · a870df77-720e-41a2-b2f7-0c5cc129b484

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1233323
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Excel Pharmaceutical Company, Ltd.

3
DateClassificationOfficeProject area
April 1, 2016NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 31, 2013NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
January 28, 2009NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Excel Pharmaceutical Company, Ltd.
  • FDA Inspection 963958 - 2016-04-01
  • FDA Inspection 819131 - 2013-01-31
  • FDA Inspection 565822 - 2009-01-28

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