FDA Import Refusal 799-1334086-5/11/1 — Artron Laboratories, Inc.

Artron Laboratories, Inc. — FEI 3005445066

The FDA refused shipment 799-1334086-5/11/1 from Artron Laboratories, Inc. (Canada) on Oct 19, 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
Oct 19, 2022
Country
Canada
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
508

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