Home / Import refusals / 799-7184971-8/10001/1

FDA Import Refusal 799-7184971-8/10001/1 — CORDX INC

CORDX INC — FEI 3040731211

The FDA refused shipment 799-7184971-8/10001/1 from CORDX INC (United States) on Nov 7, 2025. The refused product falls under Devices — COVID-19 MULTI-ANALYTE ANTIGEN DEVICE. Cited charges: 118,3280 This firm has 3 other import refusals on record.

Refusal Details

Date
Nov 7, 2025
Country
United States
Product Category
Devices
Product Code
83QMN COVID-19 MULTI-ANALYTE ANTIGEN DEVICE
Charges
118,3280

Other import refusals

FDA data resources

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.