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FDA Import Refusal AEK-9908723-7/1/5 — Dimeda Instrumente GmbH

Dimeda Instrumente GmbH — FEI 3002806816

The FDA refused shipment AEK-9908723-7/1/5 from Dimeda Instrumente GmbH (Germany) on Jul 16, 2009. The refused product falls under Devices — FORCEPS, OBSTETRICAL. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jul 16, 2009
Country
Germany
Product Category
Devices
Product Code
85HDA FORCEPS, OBSTETRICAL
Charges
118,508

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Other import refusals

FDA data resources

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