FDA Inspection 1048753 - Midmark Corporation - April 02, 2018

FDA Inspection 1048753 for Midmark Corporation on April 02, 2018. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1048753 for Midmark Corporation on April 02, 2018. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.100(a)

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Record Information

Company

Midmark Corporation

Inspection Date

April 2, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd6a54a6-e299-43aa-90e1-aefcb058ec11

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