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USA Medical LLC MARCS-CMS 631500 —

Delivery Method:
VIA Electronic Mail
Medical Devices

Recipient Name
Damon Roberts
Recipient Title
USA Medical LLC

1220 Texan Trail
Suite 205
Grapevine, TX 76051-4164
United States

Issuing Office:
Center for Devices and Radiological Health

United States

Dear Mr. Roberts,

The Food and Drug Administration has completed an evaluation of your corrective actions in response to Warning Letter #631500 dated 8/3/2022. Based on our evaluation, it appears that you have addressed the violation(s) contained in this Warning Letter. Future FDA inspections and regulatory activities will further assess the adequacy and sustainability of these corrections.

This letter does not relieve you or your firm from the responsibility of taking all necessary steps to assure sustained compliance with the Federal Food, Drug, and Cosmetic Act and its implementing regulations or with other relevant legal authority. The Agency expects you and your firm to maintain compliance and will continue to monitor your state of compliance. This letter will not preclude any future regulatory action should violations be observed during a subsequent inspection or through other means.

Jessica Mu
Compliance Branch Director
Office of Medical Devices and Radiological Health Operations
Division 3/West

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