FDA Inspection 1000020 - LabCorp CLS - January 27, 2017

FDA Inspection 1000020 for LabCorp CLS on January 27, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1000020 for LabCorp CLS on January 27, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

LabCorp CLS

Inspection Date

January 27, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 1862fabc-df6f-45dc-9d34-5b3465341131

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