FDA Import Refusal 799-6540119-2/11/1 — CAPITAL OFFICE

CAPITAL OFFICE — FEI 3021085230

The FDA refused shipment 799-6540119-2/11/1 from CAPITAL OFFICE (United Kingdom) on Mar 28, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,3280

Refusal details

Date
Mar 28, 2022
Country
United Kingdom
Product Category
Devices
Product Code
83QLW COVID-19 TEST HOME COLLECTION KIT DEVICES
Charges
118,3280

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