Home / Import refusals / AEK-8731475-0/11/1

FDA Import Refusal AEK-8731475-0/11/1 — Anhui Deepblue Medical Technology Co Ltd

Anhui Deepblue Medical Technology Co Ltd — FEI 3016447251

The FDA refused shipment AEK-8731475-0/11/1 from Anhui Deepblue Medical Technology Co Ltd (China) on March 31, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
March 31, 2021
Country
China
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
118,3280,508

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)
  • 799-0224950-6/11/1 (Mon Jan 11 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)
  • AEK-8131182-8/11/1 (Tue Dec 15 2020 00:00:00 GMT+0000 (Coordinated Universal Time) — Devices)

FDA data resources