FDA Inspection 1031605 - Janssen Biotech, Inc - October 06, 2017

FDA Inspection 1031605 for Janssen Biotech, Inc on October 06, 2017. Classification: No Action Indicated (NAI).

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Record Summary

FDA Inspection 1031605 for Janssen Biotech, Inc on October 06, 2017. Classification: No Action Indicated (NAI).

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Record Information

Company

Janssen Biotech, Inc

Inspection Date

October 6, 2017

Product Type

Devices

Office

Center for Devices and Radiological Health

ID: 53f4c49e-cf4c-49f1-9f13-dd31bb79b470

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