FDA Inspection 912665 - Weiman Products, LLC - January 29, 2015

FDA Inspection 912665 for Weiman Products, LLC on January 29, 2015. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 912665 for Weiman Products, LLC on January 29, 2015. Classification: No Action Indicated (NAI).

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Record Information

Company

Weiman Products, LLC

Inspection Date

January 29, 2015

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f7df3dda-3145-4a7d-a621-c2368ad76598

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