FDA Inspection 682310 - Philips Medizin Systeme Boeblingen Gmbh - September 23, 2010

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Record Details

This FDA Inspection record concerns Philips Medizin Systeme Boeblingen Gmbh, with an inspection on September 23, 2010, issued by the Center for Devices and Radiological Health, covering devices.

Company: Philips Medizin Systeme Boeblingen Gmbh
Inspection Date: September 23, 2010
Product Type: Devices
Office: Center for Devices and Radiological Health

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ID · 79bdbabe-0ee5-47d3-9fc9-a3d833d7e40e

Violation Codes5

21 CFR 820.100(a)21 CFR 820.18421 CFR 820.30(g)21 CFR 820.4021 CFR 820.70(i)

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