FDA Inspection 941165 — AMO (Hangzhou) Co., Ltd.

AMO (Hangzhou) Co., Ltd. — FEI 3004178847

The FDA completed an inspection of AMO (Hangzhou) Co., Ltd. on Aug 13, 2015 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
Aug 13, 2015
Fiscal Year
2015
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Hangzhou (China)

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