# Lumicell, Inc. – FDA Inspection, Aug 18, 2023

Source: https://www.keypedia.com/records/fda_inspections/lumicell-inc/ee5eb780-4d2c-4200-b170-e087d2e9cc86
Source feed: FDA_Inspections

> FDA inspection 1215178 of Lumicell, Inc., August 18, 2023. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR part 812. Form 483 issued. 1 other FDA inspection on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1215178
- Company Name: Lumicell, Inc.
- Inspection Date: 2023-08-18
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 2

## Related Documents

- [FDA Inspection 1221437 - 2023-10-16](https://www.keypedia.com/records/fda_inspections/lumicell-inc/3b5d980f-7f4c-43ff-be0c-c70938604547)

## Related Officers

- [Company Rep](https://www.keypedia.com/people/kent-a-conforti/8d3d3e82-cd97-420e-8840-df92d6eeba09)

Company: https://www.keypedia.com/companies/lumicell-inc/89f28fd8-1dfb-4e87-8b06-04d142447550

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7