FDA Inspection 1051621 - Lincotek Medical - April 02, 2018

FDA Inspection 1051621 for Lincotek Medical on April 02, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1051621 for Lincotek Medical on April 02, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Lincotek Medical

Inspection Date

April 2, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: fe39fb8d-25a5-46f5-867e-8bf3f21dc025

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