FDA Inspection 846131 - Korchek Technologies LLC - August 15, 2013

FDA Inspection 846131 for Korchek Technologies LLC on August 15, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 846131 for Korchek Technologies LLC on August 15, 2013. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Korchek Technologies LLC

Inspection Date

August 15, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f787a953-a4e7-40ed-99ab-495ceb441316

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