FDA Import Refusal 582-0086630-9/1/1 — Meditron, Inc.

Meditron, Inc. — FEI 3002584707

The FDA refused shipment 582-0086630-9/1/1 from Meditron, Inc. (Canada) on Dec 11, 2002. The refused product falls under Devices — CATHETER, PERCUTANEOUS, INTRAVASCULAR, LONG TERM. Cited charge: 118 This firm has 1 other import refusal on record.

Refusal details

Date
Dec 11, 2002
Country
Canada
Product Category
Devices
Product Code
80LJS CATHETER, PERCUTANEOUS, INTRAVASCULAR, LONG TERM
Charges
118

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