Home / Import refusals / AEK-0377824-6/12/1

FDA Import Refusal AEK-0377824-6/12/1 — Shenzhen Jamr Medical Technology Co., Ltd

Shenzhen Jamr Medical Technology Co., Ltd — FEI 3014166838

The FDA refused shipment AEK-0377824-6/12/1 from Shenzhen Jamr Medical Technology Co., Ltd (China) on February 11, 2022. The refused product falls under Devices — SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE. Cited charges: 118,3280,341,508 This firm has 2 other import refusals on record.

Refusal Details

Date
February 11, 2022
Country
China
Product Category
Devices
Product Code
74DXN SYSTEM, MEASUREMENT, BLOOD-PRESSURE, NON-INVASIVE
Charges
118,3280,341,508

Recent inspections

  • 1098117 (OAI Wed Jun 05 2019 00:00:00 GMT+0000 (Coordinated Universal Time))

Other import refusals

  • SCS-3897063-0/12/1 (Fri Feb 12 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • SCS-2253493-9/12/1 (Fri Nov 13 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources