Bodyline, Inc. – FDA Inspection, Apr 19, 2018

Record Details

This FDA Inspection record concerns Bodyline, Inc., with an inspection on April 19, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Bodyline, Inc.
Inspection Date: April 19, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health
Person: Richard K. Vogel (FDA Associated Person)

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ID · f8824375-6166-4556-b3dc-4738bd3be5b0

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1052190
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Devices

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FDA Inspection

Bodyline, Inc.April 19, 2018