FDA Inspection 1029014 — Taicang Kanghui Technology Development Company, Ltd.

Taicang Kanghui Technology Development Company, Ltd. — FEI 3007031002

The FDA completed an inspection of Taicang Kanghui Technology Development Company, Ltd. on September 21, 2017 in Suzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
September 21, 2017
Fiscal Year
2017
Product Type
Devices
Project Area
Compliance: Devices
Location
Suzhou (China)