FDA Import Refusal 112-3071951-3/1/1 — Serfib S.A.
The FDA refused shipment 112-3071951-3/1/1 from Serfib S.A. (France) on Jun 30, 2008. The refused product falls under Devices — DIRECT AGGLUTINATION TEST, TOXOPLASMA GONDII. Cited charges: 118,508
Refusal details
- Date
- Jun 30, 2008
- Country
- France
- Product Category
- Devices
- Product Code
- 83LLA DIRECT AGGLUTINATION TEST, TOXOPLASMA GONDII
- Charges
- 118,508