FDA Inspection 1218587 - DynaFlex - September 25, 2023

FDA Inspection 1218587 for DynaFlex on September 25, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1218587 for DynaFlex on September 25, 2023. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

DynaFlex

Inspection Date

September 25, 2023

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f73cc413-96b2-4adc-ad9e-f84ea9421dc5

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