FDA Import Refusal 799-7033469-3/11/1 — ABBOTT DIAGNOSTICS KOREA INC

ABBOTT DIAGNOSTICS KOREA INC — FEI 3015883679

The FDA refused shipment 799-7033469-3/11/1 from ABBOTT DIAGNOSTICS KOREA INC (South Korea) on Feb 14, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charge: 508 This firm has 3 other import refusals on record.

Refusal Details

Date
Feb 14, 2022
Country
South Korea
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.