FDA Inspection 598802 - Pierre P Leimgruber MD - June 25, 2009

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Record Details

This FDA Inspection record concerns Pierre P Leimgruber MD, with an inspection on June 25, 2009, issued by the Center for Devices and Radiological Health, covering devices.

Company: Pierre P Leimgruber MD
Inspection Date: June 25, 2009
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 14e7e54e-2246-4d88-8f5d-88d2fd5ca2a9

Violation Codes6

21 CFR 812.10021 CFR 812.110(b)21 CFR 812.140(a)(2)(ii)21 CFR 812.140(a)(3)21 CFR 812.140(a)(3)(i)21 CFR 812.140(a)(3)(ii)

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