# Versiti Illinois Inc, Aurora, IL – FDA Inspections

Source: https://www.keypedia.com/companies/versiti-illinois-inc/d435b9fd-9baa-426b-9498-748bc8bcffc9

> Inspection records and compliance data for Versiti Illinois Inc in Aurora, Illinois. 8 FDA inspections on record, last inspected January 16, 2025.

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## Details

- Name: Versiti Illinois Inc
- FEI Number: 1470274
- Address Line 1: 1200 N Highland Ave
- City: Aurora
- State: Illinois
- Zip Code: 60506
- Country Name: United States
- Address: 1200 N Highland Ave, Aurora, Illinois 60506, United States
- Country: United States

## Related Documents

- FDA Inspection 1259068 - Versiti Illinois Inc - 2025-01-16 — source: FDA, date: January 16, 2025
- FDA Inspection 1259068 - Versiti Illinois Inc - 2025-01-16 — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2025
- FDA Inspection 1180930 - Versiti Illinois Inc - 2022-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2022
- FDA Inspection 1180930 - Versiti Illinois Inc - 2022-09-15 — classification: No Action Indicated (NAI), source: FDA, date: September 15, 2022
- FDA Inspection 1045130 - Versiti Illinois Inc - 2018-01-16 — classification: No Action Indicated (NAI), source: FDA, date: January 16, 2018
- FDA Inspection 952598 - Versiti Illinois Inc - 2015-12-09 — classification: No Action Indicated (NAI), source: FDA, date: December 9, 2015
- FDA Inspection 833390 - Versiti Illinois Inc - 2013-05-29 — classification: No Action Indicated (NAI), source: FDA, date: May 29, 2013
- FDA Inspection 786668 - Versiti Illinois Inc - 2012-06-15 — classification: No Action Indicated (NAI), source: FDA, date: June 15, 2012
- FDA Inspection 727125 - Versiti Illinois Inc - 2011-05-25 — classification: No Action Indicated (NAI), source: FDA, date: May 25, 2011
- [FDA Inspection 638368 - Versiti Illinois Inc - 2010-01-14](https://www.keypedia.com/records/fda_inspections/versiti-illinois-inc/f3445b68-2892-4c2a-93a1-28d5ed1665d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: January 14, 2010

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