FDA Import Refusal 112-6125784-9/1/1 — MeKo Manufacturing E.K.
The FDA refused shipment 112-6125784-9/1/1 from MeKo Manufacturing E.K. (Germany) on Mar 30, 2012. The refused product falls under Devices — STENT, CARDIOVASCULAR. Cited charges: 118,237 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Mar 30, 2012
- Country
- Germany
- Product Category
- Devices
- Product Code
- 74MAF STENT, CARDIOVASCULAR
- Charges
- 118,237