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FDA Import Refusal 112-9824652-4/1/1 — Omx Gmbh

Omx Gmbh — FEI 3006291115

The FDA refused shipment 112-9824652-4/1/1 from Omx Gmbh (Germany) on Dec 13, 2011. The refused product falls under Devices — INSTRUMENT, MANUAL, GENERAL SURGICAL. Cited charge: 118

Refusal details

Date
Dec 13, 2011
Country
Germany
Product Category
Devices
Product Code
79MDM INSTRUMENT, MANUAL, GENERAL SURGICAL
Charges
118

FDA data resources

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