FDA Inspection 1134099 — OrbusNeich Medical (Shenzhen) Co., Ltd.

OrbusNeich Medical (Shenzhen) Co., Ltd. — FEI 3003775186

The FDA completed an inspection of OrbusNeich Medical (Shenzhen) Co., Ltd. on Dec 4, 2020 in Shenzhen. 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
Dec 4, 2020
Fiscal Year
2021
Product Type
Devices
Project Area
Compliance: Devices
Location
Shenzhen (China)

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