FDA Import Refusal 004-0083156-7/6/1 — Medtronic CryoCath LP
The FDA refused shipment 004-0083156-7/6/1 from Medtronic CryoCath LP (Canada) on Apr 19, 2017. The refused product falls under Devices — CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION. Cited charge: 508 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Apr 19, 2017
- Country
- Canada
- Product Category
- Devices
- Product Code
- 74OAE CATHETER, PERCUTANEOUS, CARDIAC ABLATION, FOR TREATMENT OF ATRIAL FIBRILLATION
- Charges
- 508