FDA Import Refusal 799-6920400-6/11/1 — Artron Laboratories, Inc.

Artron Laboratories, Inc. — FEI 3005445066

The FDA refused shipment 799-6920400-6/11/1 from Artron Laboratories, Inc. (Canada) on Feb 24, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal Details

Date
Feb 24, 2022
Country
Canada
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
237

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