FDA Import Refusal SCS-4973839-0/11/1 — TELEFLEX MEDICAL EUROPE LIMITED

TELEFLEX MEDICAL EUROPE LIMITED — FEI 3029088606

The FDA refused shipment SCS-4973839-0/11/1 from TELEFLEX MEDICAL EUROPE LIMITED (United States) on Sep 10, 2024. The refused product falls under Devices — NEEDLE, ASPIRATION AND INJECTION, REUSABLE. Cited charges: 118,341,508

Refusal Details

Date
Sep 10, 2024
Country
United States
Product Category
Devices
Product Code
79GDM NEEDLE, ASPIRATION AND INJECTION, REUSABLE
Charges
118,341,508

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