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FDA Inspection 981968 — Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant)

Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) — FEI 3010728912

The FDA completed an inspection of Zhejiang Kangle Pharmaceutical Co., Ltd (Binhai Plant) on July 22, 2016 in Wenzhou. 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
July 22, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Wenzhou (China)

Facility

Other inspections at this facility

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  • 1084107 (VAI Fri Mar 22 2019 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 866095 (NAI Fri Dec 20 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 582495 (VAI Thu Apr 23 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources