FDA Inspection 977049 — Acon Biotech (Hangzhou) Co., Ltd.

Acon Biotech (Hangzhou) Co., Ltd. — FEI 3002829675

The FDA completed an inspection of Acon Biotech (Hangzhou) Co., Ltd. on May 6, 2016 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
May 6, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Hangzhou (China)

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