# FDA Inspection 1215178 - Lumicell, Inc. - August 18, 2023

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

> FDA Inspection 1215178 for Lumicell, Inc. on August 18, 2023. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Bioresearch Monitoring
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1221437 - 2023-10-16](https://www.keypedia.com/records/fda_inspections/lumicell-inc/3b5d980f-7f4c-43ff-be0c-c70938604547)
- [FDA Inspection 1221437 - 2023-10-16](https://www.keypedia.com/records/fda_inspections/lumicell-inc/067ee250-c137-423f-8ce4-aca6d6a5746d)

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