Home / Import refusals / AEK-8131182-8/11/1

FDA Import Refusal AEK-8131182-8/11/1 — Anhui Deepblue Medical Technology Co Ltd

Anhui Deepblue Medical Technology Co Ltd — FEI 3016447251

The FDA refused shipment AEK-8131182-8/11/1 from Anhui Deepblue Medical Technology Co Ltd (China) on December 15, 2020. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
December 15, 2020
Country
China
Product Category
Devices
Product Code
83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
Charges
508

Other import refusals

  • SCS-1832125-2/14/1 (Fri Jul 25 2025 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-5347115-7/11/1 (Fri Nov 19 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • AEK-8731475-0/11/1 (Wed Mar 31 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0224950-6/11/2 (Mon Jan 11 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)
  • 799-0224950-6/11/1 (Mon Jan 11 2021 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources