FDA Import Refusal AEK-0867214-7/11/1 — ABBOTT DIAGNOSTICS

ABBOTT DIAGNOSTICS — FEI 3020654658

The FDA refused shipment AEK-0867214-7/11/1 from ABBOTT DIAGNOSTICS (South Korea) on Mar 22, 2022. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Mar 22, 2022
Country
South Korea
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508