FDA Import Refusal 112-5165495-3/1/1 — Spectralytics

Spectralytics — FEI 3004061621

The FDA refused shipment 112-5165495-3/1/1 from Spectralytics (United States) on Jan 6, 2009. The refused product falls under Devices — CATHETER, CORONARY, ACUTE MYOCARDIAL INFARCTION, TEMPORARY, FOR EMBOLIZATION PROTECTION. Cited charge: 118 This firm has 4 other import refusals on record.

Refusal Details

Date
Jan 6, 2009
Country
United States
Product Category
Devices
Product Code
74OBX CATHETER, CORONARY, ACUTE MYOCARDIAL INFARCTION, TEMPORARY, FOR EMBOLIZATION PROTECTION
Charges
118