FDA Import Refusal 112-6264353-3/2/1 — Sanofi Aventis
The FDA refused shipment 112-6264353-3/2/1 from Sanofi Aventis (France) on Aug 19, 2011. The refused product falls under Devices — NEEDLE, HYPODERMIC, SINGLE LUMEN. Cited charge: 75 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Aug 19, 2011
- Country
- France
- Product Category
- Devices
- Product Code
- 80FMI NEEDLE, HYPODERMIC, SINGLE LUMEN
- Charges
- 75