FDA Import Refusal 799-7274723-1/11/1 — MEDIMAP

MEDIMAP — FEI 3021507559

The FDA refused shipment 799-7274723-1/11/1 from MEDIMAP (United Kingdom) on Apr 5, 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
Apr 5, 2022
Country
United Kingdom
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.