# Lumitex Medical Devices Inc - Inspection Records

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

> Inspection records and compliance data for Lumitex Medical Devices Inc in Strongsville, Ohio. Access full analysis and detailed observations.

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## Details

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

## Related Documents

- [FDA Inspection 1000208 - Lumitex Medical Devices Inc - 2017-01-09](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/1646daeb-4e37-4327-a2fd-05abc9e67106) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2017
- [FDA Inspection 1000208 - Lumitex Medical Devices Inc - 2017-01-09](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/b6ad7ffd-a635-4358-9f4f-308397879d9b) — classification: No Action Indicated (NAI), source: FDA, date: January 9, 2017
- [FDA Inspection 859893 - Lumitex Medical Devices Inc - 2013-12-26](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/74a0e166-9a99-4cab-84da-0f8448e08ebb) — classification: No Action Indicated (NAI), source: FDA, date: December 26, 2013
- [FDA Inspection 859893 - Lumitex Medical Devices Inc - 2013-12-26](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/2c4907d5-2ab5-4a24-ac44-71d8b1a6f1ec) — classification: No Action Indicated (NAI), source: FDA, date: December 26, 2013
- [FDA Inspection 730676 - Lumitex Medical Devices Inc - 2011-06-22](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/68bfee18-618f-48bf-85c9-b6dcbe3c3c67) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2011
- [FDA Inspection 730676 - Lumitex Medical Devices Inc - 2011-06-22](https://www.globalkeysolutions.net/records/fda_inspections/lumitex-medical-devices-inc/fd30936b-0871-428a-aaea-5cebe0e06c04) — classification: No Action Indicated (NAI), source: FDA, date: June 22, 2011

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