FDA Import Refusal 112-6615169-9/1/1 — MeKo Manufacturing E.K.

MeKo Manufacturing E.K. — FEI 3009937642

The FDA refused shipment 112-6615169-9/1/1 from MeKo Manufacturing E.K. (Germany) on Jun 20, 2012. The refused product falls under Devices — DEVICE, TESTICULAR HYPOTHERMIA. Cited charge: 237 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 20, 2012
Country
Germany
Product Category
Devices
Product Code
78LOA DEVICE, TESTICULAR HYPOTHERMIA
Charges
237

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.