FDA Inspection 762942 - Mediagnost GmbH - January 11, 2012

FDA Inspection 762942 for Mediagnost GmbH on January 11, 2012. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 762942 for Mediagnost GmbH on January 11, 2012. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.17

21 CFR 820.120

21 CFR 820.184

21 CFR 820.40

21 CFR 820.60

21 CFR 820.70(g)

21 CFR 820.75(a)

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Record Information

Company

Mediagnost GmbH

Inspection Date

January 11, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: c69b2be7-0be3-4583-93b4-fc071d076a5b

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