FDA Import Refusal 112-6605000-6/1/1 — Portex Ltd.

Portex Ltd. — FEI 671

The FDA refused shipment 112-6605000-6/1/1 from Portex Ltd. (United Kingdom) on Jun 21, 2007. The refused product falls under Devices — TRACHEOSTOMY AND NASAL SUCTIONING KIT. Cited charge: 508 This firm has 1 other import refusal on record.

Refusal details

Date
Jun 21, 2007
Country
United Kingdom
Product Category
Devices
Product Code
79LRQ TRACHEOSTOMY AND NASAL SUCTIONING KIT
Charges
508

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