# Lumitex Medical Devices Inc, Strongsville, OH – FDA Inspections

Source: https://www.keypedia.com/companies/lumitex-medical-devices-inc/19fa724c-17a2-4f62-a576-8e27c8b303d1

> Inspection records and compliance data for Lumitex Medical Devices Inc in Strongsville, Ohio. 4 FDA inspections on record, 1 Form 483, last inspected May 01, 2026.

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## Details

- Name: Lumitex Medical Devices Inc
- FEI Number: 1000122810
- Address Line 1: 8443 Dow Cir
- City: Strongsville
- State: Ohio
- Zip Code: 44136
- Country Name: United States
- Address: 8443 Dow Cir, Strongsville, Ohio 44136, United States
- Country: United States

## Related Documents

- [483 - Lumitex Medical Devices Inc - 2026-05-01](https://www.keypedia.com/records/483/lumitex-medical-devices-inc/1c98ded3-ac37-4f93-a0e1-8303e7868bbc) — source: FDA, date: May 1, 2026
- FDA Inspection 1315326 - Lumitex Medical Devices Inc - 2026-05-01 — classification: Voluntary Action Indicated (VAI), source: FDA, date: May 1, 2026
- [FDA Inspection 1315326 - Lumitex Medical Devices Inc - 2026-05-01](https://www.keypedia.com/records/fda_inspections/lumitex-medical-devices-inc/d59a1748-59bb-48f9-90ee-10806170a1dc) — classification: No Action Indicated (NAI), source: FDA, date: May 1, 2026
- FDA Inspection 1000208 - Lumitex Medical Devices Inc - 2017-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2017
- FDA Inspection 1000208 - Lumitex Medical Devices Inc - 2017-01-09 — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2017
- FDA Inspection 859893 - Lumitex Medical Devices Inc - 2013-12-26 — classification: No Action Indicated (NAI), source: FDA, date: December 26, 2013
- FDA Inspection 859893 - Lumitex Medical Devices Inc - 2013-12-26 — classification: No Action Indicated (NAI), source: FDA, date: December 26, 2013
- FDA Inspection 730676 - Lumitex Medical Devices Inc - 2011-06-22 — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2011
- FDA Inspection 730676 - Lumitex Medical Devices Inc - 2011-06-22 — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2011

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