FDA Inspection 1084241 - ImaCor Inc. - March 26, 2019

FDA Inspection 1084241 for ImaCor Inc. on March 26, 2019. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1084241 for ImaCor Inc. on March 26, 2019. Classification: No Action Indicated (NAI).

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Record Information

Company

ImaCor Inc.

Inspection Date

March 26, 2019

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fdc80e28-4d3d-4aa1-ba25-a6b6f9fa1eb3

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