FDA Inspection 799272 - Schilling, Kathy, MD - September 18, 2012

FDA Inspection 799272 for Schilling, Kathy, MD on September 18, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 799272 for Schilling, Kathy, MD on September 18, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Schilling, Kathy, MD

Inspection Date

September 18, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc7917ed-40c0-4fc1-9e11-e067e3293438

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