FDA Inspection 904003 — Abon Biopharm (Hangzhou) Co., Ltd.

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

The FDA completed an inspection of Abon Biopharm (Hangzhou) Co., Ltd. on Nov 13, 2014 in Hangzhou. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Nov 13, 2014
Fiscal Year
2015
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.