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FDA Inspection
•Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site)•December 13, 2013

FDA Inspection 865961 - Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site) - December 13, 2013

Record Details

This FDA Inspection record concerns Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site), with an inspection on December 13, 2013, issued by the Center for Drug Evaluation and Research, covering drugs.

Company
Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site)
Inspection Date
December 13, 2013
Product Type
Drugs
Office
Center for Drug Evaluation and Research
View Company Profile

ID · 9b848d20-8689-4e55-9199-8304037512f5

Inspection Facts

Voluntary Action Indicated (VAI)

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

Inspection number
865961
FDA center
Human Drugs
Project area
Drug Quality Assurance

Other FDA inspections of Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site)

4
DateClassificationOfficeProject area
September 21, 2023VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
July 15, 2016VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
October 14, 2010NAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
November 21, 2008VAICenter for Veterinary MedicineMonitoring of Marketed Animal Drugs, Feed, and Devices
Other documents for Shaanxi Hanjiang Pharmaceutical Group Co., Ltd (Gaoxin site)
  • FDA Inspection 1218824 - 2023-09-21
  • FDA Inspection 982472 - 2016-07-15
  • FDA Inspection 697592 - 2010-10-14
  • FDA Inspection 552585 - 2008-11-21

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