FDA Inspection 586202 - Douglas, John - May 21, 2009

FDA Inspection 586202 for Douglas, John on May 21, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 586202 for Douglas, John on May 21, 2009. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Douglas, John

Inspection Date

May 21, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa2b2c61-e287-47cb-8b6d-15fda0928bdf

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