FDA Import Refusal 799-0964781-4/24/1 — Dimeda Instrumente GmbH

Dimeda Instrumente GmbH — FEI 3002806816

The FDA refused shipment 799-0964781-4/24/1 from Dimeda Instrumente GmbH (Germany) on Nov 14, 2013. The refused product falls under Devices — SPECULUM, VAGINAL, METAL. Cited charge: 118 This firm has 5 or more other import refusals on record.

Refusal details

Date
Nov 14, 2013
Country
Germany
Product Category
Devices
Product Code
85HDF SPECULUM, VAGINAL, METAL
Charges
118

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