FDA Import Refusal AEK-6982302-5/1/1 — Asamed
The FDA refused shipment AEK-6982302-5/1/1 from Asamed (Poland) on Nov 17, 2004. The refused product falls under Devices — INSTRUMENT, COAGULATION, AUTOMATED. Cited charges: 118,508 This firm has 1 other import refusal on record.
Refusal details
- Date
- Nov 17, 2004
- Country
- Poland
- Product Category
- Devices
- Product Code
- 81GKP INSTRUMENT, COAGULATION, AUTOMATED
- Charges
- 118,508