FDA Inspection 986623 — Jianerkang Medical Co., Ltd

Jianerkang Medical Co., Ltd — FEI 3006403682

The FDA completed an inspection of Jianerkang Medical Co., Ltd on April 14, 2016 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: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
April 14, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Changzhou (China)