FDA Inspection 1080165 - Kenneth Snyder, M.D. - February 13, 2019

Record Details

This FDA Inspection record concerns Kenneth Snyder, M.D., with an inspection on February 13, 2019, issued by the Center for Devices and Radiological Health, covering devices.

Company: Kenneth Snyder, M.D.
Inspection Date: February 13, 2019
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 4aa11488-a28f-4ade-87e1-80ca930895d4