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FDA Import Refusal AEK-5236371-7/11/1 — St. Jude Medical

St. Jude Medical — FEI 2182269

The FDA refused shipment AEK-5236371-7/11/1 from St. Jude Medical (United States) on November 1, 2018. The refused product falls under Devices — CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING. Cited charges: 118,3280,508

Refusal Details

Date
November 1, 2018
Country
United States
Product Category
Devices
Product Code
74DRF CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING
Charges
118,3280,508

Recent inspections

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  • 721939 (VAI Thu Apr 21 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

Compliance actions

FDA data resources