FDA Inspection 1074202 - Neal S. Kleiman, M.D. - December 06, 2018

Record Details

This FDA Inspection record concerns Neal S. Kleiman, M.D., with an inspection on December 6, 2018, issued by the Center for Devices and Radiological Health, covering devices.

Company: Neal S. Kleiman, M.D.
Inspection Date: December 6, 2018
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 6e7f99b8-b8f2-448f-8a8f-7fa8d00dd62e

Violation Codes1

21 CFR 812.110(b)

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