FDA Import Refusal 112-7548806-6/1/1 — MeKo Manufacturing E.K.
The FDA refused shipment 112-7548806-6/1/1 from MeKo Manufacturing E.K. (Germany) on Jun 11, 2012. The refused product falls under Devices — STENT, SUPERFICIAL FEMORAL ARTERY. Cited charge: 237 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Jun 11, 2012
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74NIP STENT, SUPERFICIAL FEMORAL ARTERY
- Charges
- 237