FDA Inspection 1037821 - Permobil Inc - January 11, 2018

FDA Inspection 1037821 for Permobil Inc on January 11, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1037821 for Permobil Inc on January 11, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Permobil Inc

Inspection Date

January 11, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: faf1f571-a19e-4997-90fd-74f91f986de8

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