FDA Inspection 682984 — Abon Biopharm (Hangzhou) Co., Ltd.

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

The FDA completed an inspection of Abon Biopharm (Hangzhou) Co., Ltd. on September 21, 2010 in Hangzhou. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
September 21, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)