FDA Inspection 1027670 - Dreve Otoplastik Gmbh - September 07, 2017

FDA Inspection 1027670 for Dreve Otoplastik Gmbh on September 07, 2017. Classification: Official Action Indicated (OAI).

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Record Summary

FDA Inspection 1027670 for Dreve Otoplastik Gmbh on September 07, 2017. Classification: Official Action Indicated (OAI).

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Record Information

Company

Dreve Otoplastik Gmbh

Inspection Date

September 7, 2017

Product Type

Drugs

Office

Center for Drug Evaluation and Research

ID: faeaed01-6283-4510-81d0-b5f2c7514f0c

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