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FDA Inspection
•Zhejiang Chempacific Corporation•March 23, 2018

Zhejiang Chempacific Corporation – FDA Inspection, Mar 23, 2018

Record Details

This FDA Inspection record concerns Zhejiang Chempacific Corporation, with an inspection on March 23, 2018, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Zhejiang Chempacific Corporation
Inspection Date
March 23, 2018
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Tiara N Brown-Crosen (Issuing Officer)
View Company Profile

ID · 38852223-11ec-436f-a575-a301a1e77434

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1050336
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Zhejiang Chempacific Corporation

3
DateClassificationOfficeProject area
April 4, 2025Not classifiedOffice of Inspections and Investigations
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 1268222 - 2025-04-04
  • FDA Inspection 896936 - 2014-09-04
  • FDA Inspection 728751 - 2011-05-06

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