# FDA Inspection 953250 - Versiti Illinois Inc - December 22, 2015

Source: https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/c71f41d4-30aa-41cd-ad37-1bf6d9f755c4
Source feed: FDA_Inspections

> FDA Inspection 953250 for Versiti Illinois Inc on December 22, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 953250
- Company Name: Versiti Illinois Inc
- Inspection Date: 2015-12-22
- Classification: No Action Indicated (NAI)
- Project Area: Blood and Blood Products
- Product Type: Biologics
- Office Name: Center for Biologics Evaluation and Research

## Related Documents

- [FDA Inspection 873326 - 2014-04-07](https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/568ba869-ba37-4adc-a7ac-5c227bd84e2d)
- [FDA Inspection 795183 - 2012-06-28](https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/ea8dc69a-ccc2-469c-bbe6-98f0dc121089)
- [FDA Inspection 695027 - 2010-10-25](https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/afd2fed4-ae2a-4b38-bf9b-0285cc6bea5c)
- [FDA Inspection 544726 - 2008-10-28](https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/7ac39352-8d45-4aaa-bdee-642bc089af21)

Company: https://www.keypedia.com/companies/versiti-illinois-inc/cb46d0e8-5124-4ee9-8ba3-909069442c27

Office: https://www.keypedia.com/offices/center-for-biologics-evaluation-and-research/dd9e8ea7-6f04-4ed1-b0d7-e7e6b264570d