FDA Import Refusal 310-8839222-5/1/1 — Cardia Innovation Ab
The FDA refused shipment 310-8839222-5/1/1 from Cardia Innovation Ab (United States) on Aug 9, 2007. The refused product falls under Devices — INSUFFLATOR, LAPAROSCOPIC. Cited charges: 341,508
Refusal Details
- Date
- Aug 9, 2007
- Country
- United States
- Product Category
- Devices
- Product Code
- 85HIF INSUFFLATOR, LAPAROSCOPIC
- Charges
- 341,508