FDA Import Refusal AEK-4043319-3/11/1 — PRODUCTS AND FEATURES BRASIL

PRODUCTS AND FEATURES BRASIL — FEI 3021602219

The FDA refused shipment AEK-4043319-3/11/1 from PRODUCTS AND FEATURES BRASIL (Brazil) on Oct 17, 2023. The refused product falls under Devices — DEVICE, TRANSCATHETER CARDIAC OCCLUSION. Cited charges: 118,237,3280

Refusal details

Date
Oct 17, 2023
Country
Brazil
Product Category
Devices
Product Code
74MLV DEVICE, TRANSCATHETER CARDIAC OCCLUSION
Charges
118,237,3280

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