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FDA Import Refusal 112-4122465-3/2/1 — Sanofi Aventis Spa

Sanofi Aventis Spa — FEI 3005512880

The FDA refused shipment 112-4122465-3/2/1 from Sanofi Aventis Spa (Italy) on Oct 18, 2011. The refused product falls under Devices — INTRODUCER, SYRINGE NEEDLE. Cited charges: 118,508 This firm has 5 or more other import refusals on record.

Refusal details

Date
Oct 18, 2011
Country
Italy
Product Category
Devices
Product Code
80KZH INTRODUCER, SYRINGE NEEDLE
Charges
118,508

Other import refusals

FDA data resources

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