Home / Inspections / 892301

FDA Inspection 892301 — Changzhou Qianhong Biopharma Co., Ltd.

Changzhou Qianhong Biopharma Co., Ltd. — FEI 3005275502

The FDA completed an inspection of Changzhou Qianhong Biopharma Co., Ltd. on August 1, 2014 in Changzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 1, 2014
Fiscal Year
2014
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Changzhou (China)

Facility

Other inspections at this facility

  • 1295032 (VAI Fri Oct 31 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1289802 (VAI Wed May 10 2023 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1112213 (NAI Wed Oct 23 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1037659 (VAI Fri Dec 15 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 661070 (NAI Fri Apr 30 2010 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources