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WARNING LETTER RESPONSE
•Revival Products Inc•September 3, 2020

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

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