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

Source: https://www.globalkeysolutions.net/records/fda_inspections/janssen-biotech-inc/53f4c49e-cf4c-49f1-9f13-dd31bb79b470/
Source feed: FDA_Inspections

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

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1031605
- Company Name: Janssen Biotech, Inc
- Inspection Date: 2017-10-06
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.globalkeysolutions.net/companies/janssen-biotech-inc/7d87f794-c8cc-4a2c-b985-4d62ebc2d60b

Office: https://www.globalkeysolutions.net/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7