# FDA Inspection 1221437 - Lumicell, Inc. - October 16, 2023

Source: https://www.keypedia.com/records/fda_inspections/lumicell-inc/3b5d980f-7f4c-43ff-be0c-c70938604547
Source feed: FDA_Inspections

> FDA Inspection 1221437 for Lumicell, Inc. on October 16, 2023. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1221437
- Company Name: Lumicell, Inc.
- Inspection Date: 2023-10-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- 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/067ee250-c137-423f-8ce4-aca6d6a5746d)
- [FDA Inspection 1215178 - 2023-08-18](https://www.keypedia.com/records/fda_inspections/lumicell-inc/ee5eb780-4d2c-4200-b170-e087d2e9cc86)

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