# Cerenovus, Inc. – FDA Inspection, Nov 5, 2013

Source: https://www.keypedia.com/records/fda_inspections/cerenovus-inc/eb65ab13-013c-4287-8e54-a7390ddb40d1
Source feed: FDA_Inspections

> FDA inspection 855739 of Cerenovus, Inc., November 05, 2013. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR parts 803 and 820. 5 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 855739
- Company Name: Cerenovus, Inc.
- Inspection Date: 2013-11-05
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 985968 - 2016-09-21](https://www.keypedia.com/records/fda_inspections/cerenovus-inc/acbaaf18-bd29-4ad5-8f56-fc3e8dc5004e)
- FDA Inspection 746797 - 2011-09-27
- [FDA Inspection 712819 - 2011-03-04](https://www.keypedia.com/records/fda_inspections/cerenovus-inc/e3b52dca-480c-4ba8-866b-20f07a2d2fff)
- FDA Inspection 673154 - 2010-06-17
- FDA Inspection 628600 - 2009-11-17

Company: https://www.keypedia.com/companies/cerenovus-inc/caed823f-5405-40fb-9742-072a2fdba52d

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