FDA Inspection 961418 - Koning Corporation - February 10, 2016

FDA Inspection 961418 for Koning Corporation on February 10, 2016. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 961418 for Koning Corporation on February 10, 2016. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 820.198(a)

21 CFR 820.30(i)

21 CFR 820.80(b)

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Record Information

Company

Koning Corporation

Inspection Date

February 10, 2016

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fefeef1b-d00e-4b98-94c2-d78e84e7ad67

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