FDA Import Refusal 112-0405917-0/18/1 — Inkutec Gmbh

Inkutec Gmbh — FEI 3006846433

The FDA refused shipment 112-0405917-0/18/1 from Inkutec Gmbh (Germany) on Jan 4, 2013. The refused product falls under Devices — STERILANT, MEDICAL DEVICES. Cited charge: 118

Refusal details

Date
Jan 4, 2013
Country
Germany
Product Category
Devices
Product Code
80MED STERILANT, MEDICAL DEVICES
Charges
118

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