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FDA Inspection
•Zhejiang Chempacific Corporation•April 4, 2025

Zhejiang Chempacific Corporation – FDA Inspection, Apr 4, 2025

Record Details

This FDA Inspection record concerns Zhejiang Chempacific Corporation, with an inspection on April 4, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Zhejiang Chempacific Corporation
Inspection Date
April 4, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
Person
  • Kham Phommachanh (FDA Associated Person)
View Company Profile

ID · c08e1ac6-317f-4265-be3d-a9c1e7be2bf2

Inspection Facts

Inspection number
1268222
FDA center
Human Drugs
Outcome
Form 483 issued

Other FDA inspections of Zhejiang Chempacific Corporation

3
DateClassificationOfficeProject area
March 23, 2018NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 4, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 6, 2011VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Zhejiang Chempacific Corporation
  • FDA Inspection 1050336 - 2018-03-23
  • FDA Inspection 896936 - 2014-09-04
  • FDA Inspection 728751 - 2011-05-06

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