FDA Inspection 793650 - Repro-Med Systems, Inc. - July 20, 2012

FDA Inspection 793650 for Repro-Med Systems, Inc. on July 20, 2012. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 793650 for Repro-Med Systems, Inc. on July 20, 2012. Classification: No Action Indicated (NAI).

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Record Information

Company

Repro-Med Systems, Inc.

Inspection Date

July 20, 2012

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f86f29ac-89ca-4802-8792-8fb741afb9a1

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