FDA Inspection 1200226 - Orthofix U.S. LLC - March 17, 2023

FDA Inspection 1200226 for Orthofix U.S. LLC on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1200226 for Orthofix U.S. LLC on March 17, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Orthofix U.S. LLC

Inspection Date

March 17, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd45fa5e-95e6-4ef1-8b0f-57ddbfd70097

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