FDA Inspection 551123 - Uromedica Inc. - December 19, 2008

FDA Inspection 551123 for Uromedica Inc. on December 19, 2008. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 551123 for Uromedica Inc. on December 19, 2008. Classification: No Action Indicated (NAI).

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Record Information

Company

Uromedica Inc.

Inspection Date

December 19, 2008

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fd1a82bc-484f-415e-8c93-b316fcdccb93

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