FDA Inspection 856696 - Neal S. Kleiman, M.D. - November 26, 2013

Record Details

This FDA Inspection record concerns Neal S. Kleiman, M.D., with an inspection on November 26, 2013, issued by the Center for Devices and Radiological Health, covering devices.

Company: Neal S. Kleiman, M.D.
Inspection Date: November 26, 2013
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · e4c22842-c6e7-49fd-acd6-746aa6e73a71

Violation Codes3

21 CFR 812.10021 CFR 812.140(a)(1)21 CFR 812.140(a)(3)

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