FDA Inspection 1040206 - Lincotek Medical LLC. - January 12, 2018

FDA Inspection 1040206 for Lincotek Medical LLC. on January 12, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1040206 for Lincotek Medical LLC. on January 12, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Lincotek Medical LLC.

Inspection Date

January 12, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: ffaffd4c-01e3-46b2-a33d-64a21b8be46a

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