# Cerenovus Inc – FDA Inspection, Dec 30, 2010

Source: https://www.keypedia.com/records/fda_inspections/cerenovus-inc/d646f9a4-2f38-433d-bf97-a369923e05c9
Source feed: FDA_Inspections

> FDA inspection 706633 of Cerenovus Inc, December 30, 2010. Classification: No Action Indicated (NAI). 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 706633
- Company Name: Cerenovus Inc
- Inspection Date: 2010-12-30
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

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- [FDA Inspection 870464 - 2014-03-14](https://www.keypedia.com/records/fda_inspections/cerenovus-inc/b55fff30-4c5d-4eb7-93a5-43d99511406b)

Company: https://www.keypedia.com/companies/cerenovus-inc/3123c525-3fec-4ff7-b01b-5bd7a0df42e8

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