FDA Import Refusal AWM-0019176-9/1/1 — Medtronic B.V.

Medtronic B.V. — FEI 3002807561

The FDA refused shipment AWM-0019176-9/1/1 from Medtronic B.V. (Netherlands) on Aug 21, 2012. The refused product falls under Devices — PULSE-GENERATOR, PACEMAKER, IMPLANTABLE. Cited charge: 341 This firm has 5 or more other import refusals on record.

Refusal details

Date
Aug 21, 2012
Country
Netherlands
Product Category
Devices
Product Code
74DXY PULSE-GENERATOR, PACEMAKER, IMPLANTABLE
Charges
341

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