FDA Import Refusal 799-1293140-6/11/1 — MeKo Manufacturing E.K.
The FDA refused shipment 799-1293140-6/11/1 from MeKo Manufacturing E.K. (Germany) on Sep 18, 2017. The refused product falls under Devices — STENT, CORONARY, DRUG-ELUTING. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Sep 18, 2017
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74NIQ STENT, CORONARY, DRUG-ELUTING
- Charges
- 118,3280,508