FDA Inspection 1029059 - St. Jude Medical, Atrial Fibrillation Division, Inc. - September 28, 2017

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Record Details

This FDA Inspection record concerns St. Jude Medical, Atrial Fibrillation Division, Inc., with an inspection on September 28, 2017, issued by the Center for Devices and Radiological Health, covering devices.

Company: St. Jude Medical, Atrial Fibrillation Division, Inc.
Inspection Date: September 28, 2017
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · cbc87076-b2cd-44da-a992-0691193d4505