FDA Inspection 1055321 - Metritrack Inc - May 03, 2018

FDA Inspection 1055321 for Metritrack Inc on May 03, 2018. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1055321 for Metritrack Inc on May 03, 2018. Classification: No Action Indicated (NAI).

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Record Information

Company

Metritrack Inc

Inspection Date

May 3, 2018

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: f948d8ae-f775-46c7-88f9-d7dc5dc79f1b

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