FDA Inspection 907781 — Anhui Kangda Medical Products Co., Ltd.

Anhui Kangda Medical Products Co., Ltd. — FEI 3003310007

The FDA completed an inspection of Anhui Kangda Medical Products Co., Ltd. on November 19, 2014 in Chuzhou. 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
November 19, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Chuzhou (China)