FDA Inspection 726892 - Dornier Medtech Systems GmbH - April 29, 2011

FDA Inspection 726892 for Dornier Medtech Systems GmbH on April 29, 2011. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 726892 for Dornier Medtech Systems GmbH on April 29, 2011. Classification: Official Action Indicated (OAI).

Violation Codes

21 CFR 803.17(a)(1)

21 CFR 820.100(a)

21 CFR 820.198(a)

21 CFR 820.25(b)

21 CFR 820.30(g)

21 CFR 820.30(h)

21 CFR 820.30(i)

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Record Information

Company

Dornier Medtech Systems GmbH

Inspection Date

April 29, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa64b0d1-39ab-4165-b4c1-678ece67fdb3

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