FDA Inspection 1249765 — Shenzhen Coreray Technology Co., Ltd.

Shenzhen Coreray Technology Co., Ltd. — FEI 3014233600

The FDA completed an inspection of Shenzhen Coreray Technology Co., Ltd. on Aug 6, 2024 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
Aug 6, 2024
Fiscal Year
2024
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Shenzhen (China)