FDA Inspection 1210264 - Rehabtronics Inc. - July 13, 2023

FDA Inspection 1210264 for Rehabtronics Inc. on July 13, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1210264 for Rehabtronics Inc. on July 13, 2023. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

21 CFR 820.30(i)

21 CFR 820.75(a)

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Record Information

Company

Rehabtronics Inc.

Inspection Date

July 13, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffe826b8-ece0-47f0-8534-5fa48e393212

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