FDA Inspection 624765 - Quest Diagnostics - November 10, 2009

FDA Inspection 624765 for Quest Diagnostics on November 10, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 624765 for Quest Diagnostics on November 10, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Quest Diagnostics

Inspection Date

November 10, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f6c8c6b3-67f0-4735-bc58-697f2d4af796

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