FDA Import Refusal 799-7253017-9/1/1 — Acandis Gmbh

Acandis Gmbh — FEI 3008706684

The FDA refused shipment 799-7253017-9/1/1 from Acandis Gmbh (Germany) on Oct 7, 2016. The refused product falls under Devices — TUBE, SINGLE LUMEN, W MERCURY WT BALLOON FOR INTES. INTUB. &/OR DECOMPRESSION. Cited charges: 118,3280,341,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 7, 2016
Country
Germany
Product Category
Devices
Product Code
78FEF TUBE, SINGLE LUMEN, W MERCURY WT BALLOON FOR INTES. INTUB. &/OR DECOMPRESSION
Charges
118,3280,341,508

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