FDA Inspection 1024145 - Cranial Technologies Inc - June 14, 2017

FDA Inspection 1024145 for Cranial Technologies Inc on June 14, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1024145 for Cranial Technologies Inc on June 14, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Cranial Technologies Inc

Inspection Date

June 14, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fc9f511c-d90f-483e-bfa8-57b773c60098

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