FDA Inspection 1024981 - Cormed Inc - July 19, 2017

FDA Inspection 1024981 for Cormed Inc on July 19, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1024981 for Cormed Inc on July 19, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Cormed Inc

Inspection Date

July 19, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f76acbfc-0840-4540-b595-38a3312dd52c

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