FDA Import Refusal 004-9660034-7/41/1 — Medtronic Inc
The FDA refused shipment 004-9660034-7/41/1 from Medtronic Inc (United States) on May 3, 2005. The refused product falls under Devices — SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT. Cited charge: 237 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- May 3, 2005
- Country
- United States
- Product Category
- Devices
- Product Code
- 74MIH SYSTEM, ENDOVASCULAR GRAFT, AORTIC ANEURYSM TREATMENT
- Charges
- 237