FDA Inspection 792168 — Abon Biopharm (Hangzhou) Co., Ltd.

Abon Biopharm (Hangzhou) Co., Ltd. — FEI 3005641941

The FDA completed an inspection of Abon Biopharm (Hangzhou) Co., Ltd. on July 10, 2012 in Hangzhou. 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
July 10, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)