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FDA Inspection 1027076 — Zhejiang Hisun Pharmaceutical Co., Ltd.

Zhejiang Hisun Pharmaceutical Co., Ltd. — FEI 3007719313

The FDA completed an inspection of Zhejiang Hisun Pharmaceutical Co., Ltd. on August 11, 2017 in Taizhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
August 11, 2017
Fiscal Year
2017
Product Type
Veterinary
Project Area
Pre-Approval Eval. of Animal Drugs and Food Additives
Location
Taizhou (China)

Facility

Other inspections at this facility

  • 1238621 (VAI Fri Jun 21 2024 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1096299 (VAI Fri Jun 07 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 998186 (VAI Thu Jan 19 2017 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 918008 (OAI Sat Mar 07 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 793692 (NAI Thu Jul 19 2012 00:00:00 GMT+0000 (Coordinated Universal Time))

Recent compliance actions

FDA data resources