FDA Inspection 986623 — Jianerkang Medical Co., Ltd

Jianerkang Medical Co., Ltd — FEI 3006403682

The FDA completed an inspection of Jianerkang Medical Co., Ltd on Apr 14, 2016 in Changzhou. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Devices.

Inspection Details

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

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.