FDA Import Refusal 322-1809834-5/11/1 — Comef S.P.A.
The FDA refused shipment 322-1809834-5/11/1 from Comef S.P.A. (Italy) on May 24, 2018. The refused product falls under Devices — INJECTOR AND SYRINGE, ANGIOGRAPHIC. Cited charges: 3280,3280 This firm has 1 other import refusal on record.
Refusal details
- Date
- May 24, 2018
- Country
- Italy
- Product Category
- Devices
- Product Code
- 74DXT INJECTOR AND SYRINGE, ANGIOGRAPHIC
- Charges
- 3280,3280