FDA Inspection 1270686 - Mighty Oak Medical - May 09, 2025

FDA Inspection 1270686 for Mighty Oak Medical on May 09, 2025. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1270686 for Mighty Oak Medical on May 09, 2025. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.72(a)

21 CFR 820.90(a)

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Record Information

Company

Mighty Oak Medical

Inspection Date

May 9, 2025

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbf4b452-8fe2-4602-847a-8c04dbf13be5

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