FDA Inspection 851968 - Teratech Corporation - August 28, 2013

FDA Inspection 851968 for Teratech Corporation on August 28, 2013. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 851968 for Teratech Corporation on August 28, 2013. Classification: No Action Indicated (NAI).

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Record Information

Company

Teratech Corporation

Inspection Date

August 28, 2013

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fa6fc204-d8c9-4999-a43c-8c2b8582387c

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