FDA Inspection 604723 - Michael E. Janssen - August 18, 2009

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Record Details

This FDA Inspection record concerns Michael E. Janssen, with an inspection on August 18, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Michael E. Janssen
Inspection Date: August 18, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 26156097-5078-4e35-9e8e-dbbd61dfa322

Violation Codes1

21 CFR 812.110(b)

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