FDA Inspection 1098117 — Shenzhen Jamr Medical Technology Co., Ltd

Shenzhen Jamr Medical Technology Co., Ltd — FEI 3014166838

The FDA completed an inspection of Shenzhen Jamr Medical Technology Co., Ltd on June 5, 2019 in Shenzhen. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Devices.

Inspection Details

Classification
Official Action Indicated (OAI) (OAI)
End Date
June 5, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Bioresearch Monitoring
Location
Shenzhen (China)

Additional Details

Sponsor, Contract Research Organization