FDA Inspection 609125 - Helen K. Wu, M.D. - July 22, 2009

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Record Details

This FDA Inspection record concerns Helen K. Wu, M.D., with an inspection on July 22, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Helen K. Wu, M.D.
Inspection Date: July 22, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 98637763-3c49-4a42-a25e-8316127f4a13