FDA Inspection 675554 - Bunnell, Inc. - August 06, 2010

FDA Inspection 675554 for Bunnell, Inc. on August 06, 2010. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 675554 for Bunnell, Inc. on August 06, 2010. Classification: No Action Indicated (NAI).

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Record Information

Company

Bunnell, Inc.

Inspection Date

August 6, 2010

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc7bb920-2d23-42c1-9f43-77210107a6db

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