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FDA Import Refusal 112-3610601-4/1/1 — Angiopro Gmbh

Angiopro Gmbh — FEI 3005734693

The FDA refused shipment 112-3610601-4/1/1 from Angiopro Gmbh (Germany) on Oct 7, 2011. The refused product falls under Devices — NEEDLE, ASPIRATION AND NEEDLE, REPROCESSED. Cited charge: 118

Refusal details

Date
Oct 7, 2011
Country
Germany
Product Category
Devices
Product Code
79NNC NEEDLE, ASPIRATION AND NEEDLE, REPROCESSED
Charges
118

FDA data resources

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