# FDA Inspection 1218031 - Illuminix Industries LLC - September 07, 2023

Source: https://www.keypedia.com/records/fda_inspections/illuminix-industries-llc/86980067-9b99-4057-b3ba-b5d04d6bc0cf
Source feed: FDA_Inspections

> FDA Inspection 1218031 for Illuminix Industries LLC on September 07, 2023. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1218031
- Company Name: Illuminix Industries LLC
- Inspection Date: 2023-09-07
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1278235 - 2025-08-05](https://www.keypedia.com/records/fda_inspections/illuminix-industries-llc/2979a4b4-f051-4718-bb28-7e4391dc92f2)
- [FDA Inspection 1278235 - 2025-08-05](https://www.keypedia.com/records/fda_inspections/illuminix-industries-llc/301efcf9-6754-41fa-8dbc-19e1353f79a5)
- [FDA Inspection 1218031 - 2023-09-07](https://www.keypedia.com/records/fda_inspections/illuminix-industries-llc/c4fb0824-903d-460a-b45b-6170b6efe3e7)

Company: https://www.keypedia.com/companies/illuminix-industries-llc/5b69b438-61fb-454d-a3df-0e245251f06f

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