FDA Inspection 685755 - JK Products & Services, Inc - September 16, 2010

FDA Inspection 685755 for JK Products & Services, Inc on September 16, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 685755 for JK Products & Services, Inc on September 16, 2010. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

JK Products & Services, Inc

Inspection Date

September 16, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f9eaff02-cfb2-4809-a47e-d74e1b4f36da

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