FDA Inspection 1091387 - Hoosier, Inc - May 31, 2019

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Record Details

This FDA Inspection record concerns Hoosier, Inc, with an inspection on May 31, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Hoosier, Inc
Inspection Date: May 31, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e7d57146-3a6e-4b69-bb7c-c82513c79783

Violation Codes1

21 CFR 820.100(b)

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