WARNING LETTER RESPONSE
Revival Products IncRevival Products Inc – FDA Warning Letter Response, Sep 3, 2020
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.
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ID · 45804f93-ea0f-4554-b557-ebfdc3b216f8
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