FDA Import Refusal 799-0151844-9/11/1A — Citest Diagnostics Inc

Citest Diagnostics Inc — FEI 3023296261

The FDA refused shipment 799-0151844-9/11/1A from Citest Diagnostics Inc (Canada) on Aug 11, 2022. The refused product falls under Devices — COVID-19 TEST HOME COLLECTION KIT DEVICES. Cited charges: 118,3280

Refusal details

Date
Aug 11, 2022
Country
Canada
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.