FDA Inspection 1011040 - Prollenium Medical Technologies Inc. - April 20, 2017

FDA Inspection 1011040 for Prollenium Medical Technologies Inc. on April 20, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1011040 for Prollenium Medical Technologies Inc. on April 20, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Prollenium Medical Technologies Inc.

Inspection Date

April 20, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: d8e093dd-42be-47b9-a09d-6500aaa9a495

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