# FDA Inspection 959787 - Cerus Corporation - December 15, 2015

Source: https://www.keypedia.com/records/fda_inspections/cerus-corporation/c9a964ec-49bb-442b-acec-e3a5a42bef01
Source feed: FDA_Inspections

> FDA Inspection 959787 for Cerus Corporation on December 15, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 959787
- Company Name: Cerus Corporation
- Inspection Date: 2015-12-15
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 959787 - 2015-12-15](https://www.keypedia.com/records/fda_inspections/cerus-corporation/b6f8c0c1-e304-4788-a169-f6720d96c7c0)

Company: https://www.keypedia.com/companies/cerus-corporation/626302fc-cdf9-4e5c-bb3b-0960963a2ac9

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