FDA WARNING_LETTER_RESPONSE - Revival Products Inc - September 03, 2020

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Record Details

This WARNING LETTER RESPONSE record concerns Revival Products Inc, with an inspection on September 3, 2020, issued by the Office of Health Technology 5 (Neurological and Physical Medicine Devices), covering devices.

Company: Revival Products Inc
Inspection Date: September 3, 2020
Product Type: Devices
Office: Office of Health Technology 5 (Neurological and Physical Medicine Devices)
People: Patricia F. Hudson
Suzanne Tabor

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ID · 45804f93-ea0f-4554-b557-ebfdc3b216f8