FDA Import Refusal 799-0351778-5/11/1 — Intermedic Arfran S.A.
The FDA refused shipment 799-0351778-5/11/1 from Intermedic Arfran S.A. (Spain) on March 4, 2019. The refused product falls under Devices — SYSTEM, PERFUSION, KIDNEY. Cited charge: 118 This firm has 1 other import refusal on record.
Refusal Details
- Date
- March 4, 2019
- Country
- Spain
- Product Category
- Devices
- Product Code
- 78KDN SYSTEM, PERFUSION, KIDNEY
- Charges
- 118