FDA Import Refusal 508-0381213-5/101/8 — CORDIS DE MEXICO, SA DE CV
The FDA refused shipment 508-0381213-5/101/8 from CORDIS DE MEXICO, SA DE CV (Mexico) on Jun 3, 2019. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charge: 341 This firm has 4 other import refusals on record.
Refusal Details
- Date
- Jun 3, 2019
- Country
- Mexico
- Product Category
- Devices
- Product Code
- 74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
- Charges
- 341