FDA Import Refusal 004-5998192-4/3/1 — Medtronic Inc
The FDA refused shipment 004-5998192-4/3/1 from Medtronic Inc (United States) on Aug 10, 2011. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Aug 10, 2011
- Country
- United States
- Product Category
- Devices
- Product Code
- 74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
- Charges
- 508