# Loyola Univ Medical Center, Maywood, IL – FDA Inspections

Source: https://www.keypedia.com/companies/loyola-univ-medical-center/e2f3c4fb-ff88-44f5-b038-d0cfbf05820b

> Inspection records and compliance data for Loyola Univ Medical Center in Maywood, Illinois. 7 FDA inspections on record, 1 Form 483, last inspected September 08, 2025.

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## Details

- Name: Loyola Univ Medical Center
- FEI Number: 1475369
- Address Line 1: 2160 S 1st Ave
- City: Maywood
- State: Illinois
- Zip Code: 60153
- Country Name: United States
- Address: 2160 S 1st Ave, Maywood, Illinois 60153, United States
- Country: United States

## Related Documents

- FDA Inspection 1281146 - Loyola Univ Medical Center - 2025-09-08 — source: FDA, date: September 8, 2025
- FDA Inspection 1281146 - Loyola Univ Medical Center - 2025-09-08 — classification: No Action Indicated (NAI), source: FDA, date: September 8, 2025
- [483 - Loyola Univ Medical Center - 2024-12-05](https://www.keypedia.com/records/483/loyola-univ-medical-center/bd362a1e-9591-4c5b-b33f-904e03f745f7) — source: FDA, date: December 5, 2024
- [FDA Inspection 1255837 - Loyola Univ Medical Center - 2024-12-05](https://www.keypedia.com/records/fda_inspections/loyola-univ-medical-center/d081d0f8-e961-41f0-bc54-254cad1ac96a) — classification: Voluntary Action Indicated (VAI), source: FDA, date: December 5, 2024
- FDA Inspection 1106929 - Loyola Univ Medical Center - 2019-09-20 — classification: No Action Indicated (NAI), source: FDA, date: September 20, 2019
- FDA Inspection 1008776 - Loyola Univ Medical Center - 2017-03-23 — classification: No Action Indicated (NAI), source: FDA, date: March 23, 2017
- FDA Inspection 913470 - Loyola Univ Medical Center - 2015-02-05 — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 5, 2015
- FDA Inspection 831806 - Loyola Univ Medical Center - 2013-05-03 — classification: No Action Indicated (NAI), source: FDA, date: May 3, 2013
- FDA Inspection 679330 - Loyola Univ Medical Center - 2010-08-16 — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2010

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