FDA Inspection 1000600 - Grimm Scientific Industries - January 13, 2017

FDA Inspection 1000600 for Grimm Scientific Industries on January 13, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Summary

FDA Inspection 1000600 for Grimm Scientific Industries on January 13, 2017. Classification: Voluntary Action Indicated (VAI).

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Record Information

Company

Grimm Scientific Industries

Inspection Date

January 13, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: c4123f12-32ed-43c5-b366-b8c09a6d8cc5

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