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FDA Import Refusal AV1-0791025-7/5/1 — Dimeda Instrumente GmbH

Dimeda Instrumente GmbH — FEI 3002806816

The FDA refused shipment AV1-0791025-7/5/1 from Dimeda Instrumente GmbH (Germany) on Jul 29, 2009. The refused product falls under Devices — CANNULA, SUCTION, UTERINE. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 29, 2009
Country
Germany
Product Category
Devices
Product Code
85HGH CANNULA, SUCTION, UTERINE
Charges
508

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FDA data resources

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