FDA Inspection 808378 - Precision Interconnect, LLC - November 13, 2012

FDA Inspection 808378 for Precision Interconnect, LLC on November 13, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 808378 for Precision Interconnect, LLC on November 13, 2012. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Precision Interconnect, LLC

Inspection Date

November 13, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fbe8697e-a935-48f7-b21a-e35e10eed9ee

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