FDA Import Refusal 112-7300460-0/1/1 — St. Jude Medical, Atrial Fibrillation Division, Inc.

St. Jude Medical, Atrial Fibrillation Division, Inc. — FEI 1000139754

The FDA refused shipment 112-7300460-0/1/1 from St. Jude Medical, Atrial Fibrillation Division, Inc. (United States) on July 8, 2010. The refused product falls under Devices — DEVICE, GENERAL MEDICAL. Cited charge: 118

Refusal Details

Date
July 8, 2010
Country
United States
Product Category
Devices
Product Code
80LDQ DEVICE, GENERAL MEDICAL
Charges
118