FDA Import Refusal 799-4028702-6/1/1 — Neu-Tec Gmbh

Neu-Tec Gmbh — FEI 3010584719

The FDA refused shipment 799-4028702-6/1/1 from Neu-Tec Gmbh (Germany) on May 22, 2014. The refused product falls under Devices — NEBULIZER (DIRECT PATIENT INTERFACE). Cited charge: 3260

Refusal details

Date
May 22, 2014
Country
Germany
Product Category
Devices
Product Code
73CAF NEBULIZER (DIRECT PATIENT INTERFACE)
Charges
3260

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