FDA Import Refusal 112-0108835-3/3/1 — EKF Diagnostic Gmbh

EKF Diagnostic Gmbh — FEI 3004838836

The FDA refused shipment 112-0108835-3/3/1 from EKF Diagnostic Gmbh (Germany) on May 24, 2012. The refused product falls under Devices — SINGLE (SPECIFIED) ANALYTE CONTROLS (ASSAYED AND UNASSAYED). Cited charge: 118 This firm has 3 other import refusals on record.

Refusal details

Date
May 24, 2012
Country
Germany
Product Category
Devices
Product Code
75JJX SINGLE (SPECIFIED) ANALYTE CONTROLS (ASSAYED AND UNASSAYED)
Charges
118

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