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FDA Inspection
•Jiangsu Weiqida Pharmaceutical Co., Ltd.•December 15, 2017

Jiangsu Weiqida Pharmaceutical Co., Ltd. – FDA Inspection, Dec 15, 2017

Record Details

This FDA Inspection record concerns Jiangsu Weiqida Pharmaceutical Co., Ltd., with an inspection on December 15, 2017, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Jiangsu Weiqida Pharmaceutical Co., Ltd.
Inspection Date
December 15, 2017
Product Type
Drugs
Office
Center for Drug Evaluation and Research
Person
  • Steven P Donald (Issuing Officer)
View Company Profile

ID · ab5f8eda-6119-432b-8290-67fa2cfe855a

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
1038055
FDA center
Human Drugs
Project area
Drug Quality Assurance
Outcome
Form 483 issued

Other FDA inspections of Jiangsu Weiqida Pharmaceutical Co., Ltd.

2
DateClassificationOfficeProject area
March 21, 2025Not classifiedOffice of Inspections and Investigations
April 30, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Jiangsu Weiqida Pharmaceutical Co., Ltd.
  • FDA Inspection 1265662 - 2025-03-21
  • FDA Inspection 880208 - 2014-04-30

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