FDA Import Refusal AEK-8858565-4/1/1 — De Sisti Lighing Srl

De Sisti Lighing Srl — FEI 1000322291

The FDA refused shipment AEK-8858565-4/1/1 from De Sisti Lighing Srl (Italy) on Nov 7, 2011. The refused product falls under Devices — DEVICE, DISCHARGE, ELECTROSTATIC (FOR PAIN RELIEF). Cited charges: 118,126,508

Refusal details

Date
Nov 7, 2011
Country
Italy
Product Category
Devices
Product Code
84NHH DEVICE, DISCHARGE, ELECTROSTATIC (FOR PAIN RELIEF)
Charges
118,126,508

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