FDA Import Refusal 112-2123917-6/1/1 — Ikentani Company

Ikentani Company — FEI 3003996146

The FDA refused shipment 112-2123917-6/1/1 from Ikentani Company (Japan) on Aug 23, 2011. The refused product falls under Devices — LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION). Cited charge: 235

Refusal details

Date
Aug 23, 2011
Country
Japan
Product Category
Devices
Product Code
86HQG LENS, SPECTACLE, NON-CUSTOM (PRESCRIPTION)
Charges
235

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