FDA Import Refusal AEK-5975072-6/11/1 — Sanofi Aventis Spa
The FDA refused shipment AEK-5975072-6/11/1 from Sanofi Aventis Spa (Italy) on Jun 12, 2019. The refused product falls under Drugs and Biologics — HEPARIN SODIUM (ANTI-COAGULANT). Cited charges: 472,75 This firm has 5 or more other import refusals on record.
Refusal details
- Date
- Jun 12, 2019
- Country
- Italy
- Product Category
- Drugs and Biologics
- Product Code
- 61LBO08 HEPARIN SODIUM (ANTI-COAGULANT)
- Charges
- 472,75