FDA Inspection 630114 - Westmed, Inc. - November 05, 2009

FDA Inspection 630114 for Westmed, Inc. on November 05, 2009. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 630114 for Westmed, Inc. on November 05, 2009. Classification: No Action Indicated (NAI).

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Record Information

Company

Westmed, Inc.

Inspection Date

November 5, 2009

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffd11a80-85b3-4dae-a17a-f85849f23ef9

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