FDA Inspection 913895 - Sunpentown International Inc - February 12, 2015

FDA Inspection 913895 for Sunpentown International Inc on February 12, 2015. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 913895 for Sunpentown International Inc on February 12, 2015. Classification: Voluntary Action Indicated (VAI).

Violation Codes

21 CFR 803.17

21 CFR 820.198(a)

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Record Information

Company

Sunpentown International Inc

Inspection Date

February 12, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f82fbb1b-8e83-492a-ac83-1ded60eee727

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