FDA Import Refusal 112-6933651-2/1/1 — A.L.T. Lichttherapietechnik Gmbh

A.L.T. Lichttherapietechnik Gmbh — FEI 3003865000

The FDA refused shipment 112-6933651-2/1/1 from A.L.T. Lichttherapietechnik Gmbh (Germany) on Jun 8, 2012. The refused product falls under Devices — DEVICE, IONTOPHORESIS, SPECIFIC USES. Cited charges: 16,508,84 This firm has 1 other import refusal on record.

Refusal details

Date
Jun 8, 2012
Country
Germany
Product Category
Devices
Product Code
89KTB DEVICE, IONTOPHORESIS, SPECIFIC USES
Charges
16,508,84

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