FDA Inspection 975320 — Amsino Medical (Kunshan) Co., Ltd.

Amsino Medical (Kunshan) Co., Ltd. — FEI 3005669815

The FDA completed an inspection of Amsino Medical (Kunshan) Co., Ltd. on May 12, 2016 in Suzhou. 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 12, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Compliance: Devices
Location
Suzhou (China)

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