FDA Inspection 719704 - Heraeus Kulzer GmbH - March 10, 2011

FDA Inspection 719704 for Heraeus Kulzer GmbH on March 10, 2011. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 719704 for Heraeus Kulzer GmbH on March 10, 2011. Classification: Official Action Indicated (OAI).

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Record Information

Company

Heraeus Kulzer GmbH

Inspection Date

March 10, 2011

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fb261a0e-bf95-47ab-ab61-992cd15548f5

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