# Eversight Illinois, Chicago, IL – FDA Inspections

Source: https://www.keypedia.com/companies/eversight-illinois/7b7a3e81-0ca7-4d57-b230-5dc8e929c6a6

> Inspection records and compliance data for Eversight Illinois in Chicago, Illinois. 6 FDA inspections on record, last inspected June 18, 2024.

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## Details

- Name: Eversight Illinois
- FEI Number: 3001451642
- Address Line 1: 924 W 19th Pl Unit 350
- City: Chicago
- State: Illinois
- Zip Code: 60608
- Country Name: United States
- Address: 924 W 19th Pl Unit 350, Chicago, Illinois 60608, United States
- Country: United States

## Related Documents

- [483 - Eversight Illinois - 2024-06-18](https://www.keypedia.com/records/483/eversight-illinois/3f350007-7c6d-4557-93b1-b3d55b557341) — source: FDA, date: June 18, 2024
- [483 - Eversight Illinois - 2024-06-18](https://www.keypedia.com/records/483/eversight-illinois/f246397e-f61a-465c-b450-70f96751a4e2) — source: FDA, date: June 18, 2024
- [FDA Inspection 1241628 - Eversight Illinois - 2024-06-18](https://www.keypedia.com/records/fda_inspections/eversight-illinois/bcb4d369-162e-4484-8bcd-d4a62c2666d9) — classification: Voluntary Action Indicated (VAI), source: FDA, date: June 18, 2024
- FDA Inspection 1055320 - Eversight Illinois - 2018-04-18 — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2018
- [FDA Inspection 1055320 - Eversight Illinois - 2018-04-18](https://www.keypedia.com/records/fda_inspections/eversight-illinois/581c8d56-785a-472c-89cd-9c2899524865) — classification: No Action Indicated (NAI), source: FDA, date: April 18, 2018
- FDA Inspection 968460 - Eversight Illinois - 2016-05-09 — classification: No Action Indicated (NAI), source: FDA, date: May 9, 2016
- FDA Inspection 883885 - Eversight Illinois - 2014-06-18 — classification: No Action Indicated (NAI), source: FDA, date: June 18, 2014
- FDA Inspection 759437 - Eversight Illinois - 2011-12-19 — classification: No Action Indicated (NAI), source: FDA, date: December 19, 2011
- FDA Inspection 634088 - Eversight Illinois - 2009-12-03 — classification: No Action Indicated (NAI), source: FDA, date: December 3, 2009

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