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FDA Inspection
•Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)•October 31, 2025

Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant) – FDA Inspection, Oct 31, 2025

Record Details

This FDA Inspection record concerns Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant), with an inspection on October 31, 2025, issued by the Office of Inspections and Investigations, covering animal drugs & feeds.

Company
Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)
Inspection Date
October 31, 2025
Product Type
Animal Drugs & Feeds
Office
Office of Inspections and Investigations
Person
  • Lisa R. Hilliard (FDA Associated Person)
View Company Profile

ID · a107f5e8-8320-4d71-8b2e-dcd2dfecc209

Inspection Facts

Inspection number
1295032
FDA center
Animal Drugs & Feeds
Outcome
Form 483 issued

Other FDA inspections of Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)

5
DateClassificationOfficeProject area
May 10, 2023VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
October 23, 2019NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
December 15, 2017VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
August 1, 2014VAICenter for Drug Evaluation and ResearchDrug Quality Assurance
April 30, 2010NAICenter for Drug Evaluation and ResearchDrug Quality Assurance
Other documents for Changzhou Qianhong Bio Pharma Co., Ltd. (Formulation Plant)
  • FDA Inspection 1289802 - 2023-05-10
  • FDA Inspection 1112213 - 2019-10-23
  • FDA Inspection 1037659 - 2017-12-15
  • FDA Inspection 892301 - 2014-08-01
  • FDA Inspection 661070 - 2010-04-30

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