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FDA Inspection 1037659 — Changzhou Qianhong Biopharma Co., Ltd.

Changzhou Qianhong Biopharma Co., Ltd. — FEI 3005275502

The FDA completed an inspection of Changzhou Qianhong Biopharma Co., Ltd. on December 15, 2017 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
December 15, 2017
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Changzhou (China)

Facility

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  • 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))
  • 892301 (VAI Fri Aug 01 2014 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