FDA Inspection 790026 - Damien Sanderlin, MD - July 18, 2012

FDA Inspection 790026 for Damien Sanderlin, MD on July 18, 2012. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 790026 for Damien Sanderlin, MD on July 18, 2012. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 812.100

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Record Information

Company

Damien Sanderlin, MD

Inspection Date

July 18, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: c0ef4d71-a730-4bf1-b9f9-ba6dc73fb184

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