FDA Import Refusal AEK-8805352-2/11/1 — AEROPROFESSIONAL

AEROPROFESSIONAL — FEI 3017988196

The FDA refused shipment AEK-8805352-2/11/1 from AEROPROFESSIONAL (United Kingdom) on Mar 5, 2021. The refused product falls under Devices — CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.. Cited charges: 118,3280,508

Refusal details

Date
Mar 5, 2021
Country
United Kingdom
Product Category
Devices
Product Code
83QKP CORONAVIRUS ANTIGEN DETECTION TEST SYSTEM.
Charges
118,3280,508

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