FDA Import Refusal 799-0313648-4/1/3 — Acandis Gmbh

Acandis Gmbh — FEI 3008706684

The FDA refused shipment 799-0313648-4/1/3 from Acandis Gmbh (Germany) on Jun 18, 2015. The refused product falls under Devices — HEMODIALYSIS CATHETER LUER END CAP. Cited charges: 118,3280,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Jun 18, 2015
Country
Germany
Product Category
Devices
Product Code
78PEH HEMODIALYSIS CATHETER LUER END CAP
Charges
118,3280,508

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