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

EKF Diagnostic Gmbh — FEI 3004838836

The FDA refused shipment 112-0108835-3/1/1 from EKF Diagnostic Gmbh (Germany) on May 24, 2012. The refused product falls under Devices — GLUCOSE OXIDASE, GLUCOSE. 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
75CGA GLUCOSE OXIDASE, GLUCOSE
Charges
118

Other import refusals

FDA data resources

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