FDA Import Refusal AEK-0796009-6/1/1 — Cilag AG

Cilag AG — FEI 3002806695

The FDA refused shipment AEK-0796009-6/1/1 from Cilag AG (Switzerland) on April 10, 2015. The refused product falls under Devices — INSTRUMENT, MANUAL, GENERAL SURGICAL. Cited charges: 341,508 This firm has 5 or more other import refusals on record.

Refusal Details

Date
April 10, 2015
Country
Switzerland
Product Category
Devices
Product Code
79MDM INSTRUMENT, MANUAL, GENERAL SURGICAL
Charges
341,508