FDA Import Refusal AEK-9200784-4/1/1 — Lucio Mele Elettromedicali
The FDA refused shipment AEK-9200784-4/1/1 from Lucio Mele Elettromedicali (Italy) on Aug 7, 2013. The refused product falls under Devices — SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC. Cited charges: 118,341
Refusal details
- Date
- Aug 7, 2013
- Country
- Italy
- Product Category
- Devices
- Product Code
- 90IYN SYSTEM, IMAGING, PULSED DOPPLER, ULTRASONIC
- Charges
- 118,341