# Elmed Incorporated, Glendale Heights, IL – FDA Inspections

Source: https://www.keypedia.com/companies/elmed-incorporated/f3366bb2-c0d3-421e-b5e8-745604783131

> Inspection records and compliance data for Elmed Incorporated in Glendale Heights, Illinois. 6 FDA inspections on record, 1 Form 483, last inspected July 17, 2023.

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## Details

- Name: Elmed Incorporated
- FEI Number: 1412854
- Address Line 1: 35 N Brandon Dr
- City: Glendale Heights
- State: Illinois
- Zip Code: 60139
- Country Name: United States
- Address: 35 N Brandon Dr, Glendale Heights, Illinois 60139, United States
- Country: United States

## Related Documents

- [FDA Inspection 1210243 - Elmed Incorporated - 2023-07-17](https://www.keypedia.com/records/fda_inspections/elmed-incorporated/b4d5b5fb-7c05-4105-aec5-12be1dd95dc8) — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2023
- FDA Inspection 1210243 - Elmed Incorporated - 2023-07-17 — classification: Voluntary Action Indicated (VAI), source: FDA, date: July 17, 2023
- FDA Inspection 1088027 - Elmed Incorporated - 2019-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2019
- FDA Inspection 1088027 - Elmed Incorporated - 2019-04-12 — classification: No Action Indicated (NAI), source: FDA, date: April 12, 2019
- FDA Inspection 986692 - Elmed Incorporated - 2016-09-21 — classification: No Action Indicated (NAI), source: FDA, date: September 21, 2016
- FDA Inspection 891957 - Elmed Incorporated - 2014-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2014
- FDA Inspection 891957 - Elmed Incorporated - 2014-08-12 — classification: No Action Indicated (NAI), source: FDA, date: August 12, 2014
- FDA Inspection 712807 - Elmed Incorporated - 2011-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2011
- FDA Inspection 712807 - Elmed Incorporated - 2011-03-07 — classification: No Action Indicated (NAI), source: FDA, date: March 7, 2011
- FDA Inspection 590843 - Elmed Incorporated - 2009-06-17 — classification: No Action Indicated (NAI), source: FDA, date: June 17, 2009

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