# Lumitex Medical Devices Inc – FDA Inspection, May 1, 2026

Source: https://www.keypedia.com/records/fda_inspections/lumitex-medical-devices-inc/d59a1748-59bb-48f9-90ee-10806170a1dc
Source feed: FDA_Inspections

> FDA inspection 1315326 of Lumitex Medical Devices Inc, May 01, 2026. Classification: No Action Indicated (NAI). 2 citations. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1315326
- Company Name: Lumitex Medical Devices Inc
- Inspection Date: 2026-05-01
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Cincinnati District Office
- Citation Count: 2

## Related Documents

- FDA Inspection 1000208 - 2017-01-09
- FDA Inspection 859893 - 2013-12-26
- FDA Inspection 730676 - 2011-06-22

## Related Officers

- [Company Rep](https://www.keypedia.com/people/javonica-f-penn/56294265-08fc-4d1d-8a34-626fc4dad457)

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

Office: https://www.keypedia.com/offices/cincinnati-district-office/b67a0c35-82e3-4176-9039-988378f65c22