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FDA Inspection
•Ningxia Qiyuan Pharmaceutical Co., Ltd.•September 12, 2025

Ningxia Qiyuan Pharmaceutical Co., Ltd. – FDA Inspection, Sep 12, 2025

Record Details

This FDA Inspection record concerns Ningxia Qiyuan Pharmaceutical Co., Ltd., with an inspection on September 12, 2025, issued by the Office of Inspections and Investigations, covering human drugs.

Company
Ningxia Qiyuan Pharmaceutical Co., Ltd.
Inspection Date
September 12, 2025
Product Type
Human Drugs
Office
Office of Inspections and Investigations
People
  • Evan Tong
  • Victoria Spivak (FDA Associated Person)
View Company Profile

ID · 59d506fe-ce34-4446-82c1-d1ad672e327b

Inspection Facts

Inspection number
1288410
FDA center
Human Drugs
Outcome
Form 483 issued, view the record

Other FDA inspections of Ningxia Qiyuan Pharmaceutical Co., Ltd.

6
DateClassificationOfficeProject area
June 28, 2019VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 28, 2016VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 12, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
September 28, 2012VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
May 6, 2009VAICenter for Veterinary MedicinePre-Approval Eval. of Animal Drugs and Food Additives
View all 6 other inspections on the company page
Other documents for Ningxia Qiyuan Pharmaceutical Co., Ltd.
  • FDA Inspection 1097755 - 2019-06-28
  • FDA Inspection 968192 - 2016-04-28
  • FDA Inspection 901778 - 2014-09-12
  • FDA Inspection 801709 - 2012-09-28
  • FDA Inspection 608319 - 2009-05-06

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