FDA Import Refusal ML5-0830526-5/22/1 — Dimeda Instrumente GmbH

Dimeda Instrumente GmbH — FEI 3002806816

The FDA refused shipment ML5-0830526-5/22/1 from Dimeda Instrumente GmbH (Germany) on Nov 18, 2003. The refused product falls under Devices — DILATOR, VAGINAL. Cited charge: 508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Nov 18, 2003
Country
Germany
Product Category
Devices
Product Code
85HDX DILATOR, VAGINAL
Charges
508

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