FDA Import Refusal AEK-1898225-4/41/1 — BTNX Inc.

BTNX Inc. — FEI 3003917514

The FDA refused shipment AEK-1898225-4/41/1 from BTNX Inc. (Canada) on Oct 11, 2022. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,3280,341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 11, 2022
Country
Canada
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
118,3280,341

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