FDA Import Refusal 799-7074906-4/21/1 — ABBOTT RAPID DIAGNOSTICS ULC

ABBOTT RAPID DIAGNOSTICS ULC — FEI 3016598932

The FDA refused shipment 799-7074906-4/21/1 from ABBOTT RAPID DIAGNOSTICS ULC (Canada) on Mar 10, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 1 other import refusal on record.

Refusal details

Date
Mar 10, 2022
Country
Canada
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
508

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