FDA Import Refusal 112-5676690-2/1/1 — MeKo Manufacturing E.K.

MeKo Manufacturing E.K. — FEI 3009937642

The FDA refused shipment 112-5676690-2/1/1 from MeKo Manufacturing E.K. (Germany) on Jun 8, 2011. The refused product falls under Devices — TUBE, GASTRO-ENTEROSTOMY. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 8, 2011
Country
Germany
Product Category
Devices
Product Code
78KGC TUBE, GASTRO-ENTEROSTOMY
Charges
118

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