# FDA Inspection 985968 - Cerenovus, Inc. - September 21, 2016

Source: https://www.globalkeysolutions.net/records/fda_inspections/cerenovus-inc/a23f89eb-d88c-4e3f-9278-0ca4f7c5bc29
Source feed: FDA_Inspections

> FDA Inspection 985968 for Cerenovus, Inc. on September 21, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985968
- Company Name: Cerenovus, Inc.
- Inspection Date: 2016-09-21
- Classification: No Action Indicated (NAI)
- Project Area: Radiation Control and Health Safety Act
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 985968 - 2016-09-21](https://www.globalkeysolutions.net/records/fda_inspections/cerenovus-inc/acbaaf18-bd29-4ad5-8f56-fc3e8dc5004e)
- [FDA Inspection 855739 - 2013-11-05](https://www.globalkeysolutions.net/records/fda_inspections/cerenovus-inc/eb65ab13-013c-4287-8e54-a7390ddb40d1)
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Company: https://www.globalkeysolutions.net/companies/cerenovus-inc/caed823f-5405-40fb-9742-072a2fdba52d

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