FDA Import Refusal 799-9720196-2/11/1 — Reimers & Janssen Gmbh

Reimers & Janssen Gmbh — FEI 3008653044

The FDA refused shipment 799-9720196-2/11/1 from Reimers & Janssen Gmbh (Germany) on Mar 31, 2017. The refused product falls under Devices — LIGHT, LYMPHADEMA REDUCTION, LOW ENERGY. Cited charges: 118,3280 This firm has 5 or more other import refusals on record.

Refusal details

Date
Mar 31, 2017
Country
Germany
Product Category
Devices
Product Code
84NZY LIGHT, LYMPHADEMA REDUCTION, LOW ENERGY
Charges
118,3280

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