FDA Inspection 979706 — Jiangyin PureMED Products Co., Ltd.

Jiangyin PureMED Products Co., Ltd. — FEI 3008352384

The FDA completed an inspection of Jiangyin PureMED Products Co., Ltd. on March 31, 2016 in Jiangyin. 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
March 31, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Jiangyin (China)