FDA Import Refusal 231-7954816-2/1/18 — Arrow International CR, A.S.
The FDA refused shipment 231-7954816-2/1/18 from Arrow International CR, A.S. (Czech Republic) on Apr 20, 2015. The refused product falls under Devices — CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL. Cited charge: 118 This firm has 5 or more other import refusals on record.
Refusal Details
- Date
- Apr 20, 2015
- Country
- Czech Republic
- Product Category
- Devices
- Product Code
- 74LIT CATHETER, ANGIOPLASTY, PERIPHERAL, TRANSLUMINAL
- Charges
- 118