# FDA Inspection 1229357 - Lumendi, LLC - January 16, 2024

Source: https://www.keypedia.com/records/fda_inspections/lumendi-llc/53296470-abbd-4676-8dd3-600542db6ce9
Source feed: FDA_Inspections

> FDA Inspection 1229357 for Lumendi, LLC on January 16, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1229357
- Company Name: Lumendi, LLC
- Inspection Date: 2024-01-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1229357 - 2024-01-16](https://www.keypedia.com/records/fda_inspections/lumendi-llc/a468bbbc-ba43-4ddf-87e9-92434554ee04)
- [FDA Inspection 1073774 - 2018-11-28](https://www.keypedia.com/records/fda_inspections/lumendi-llc/700cb679-a168-43ee-83b1-735266052b5f)
- [FDA Inspection 1073774 - 2018-11-28](https://www.keypedia.com/records/fda_inspections/lumendi-llc/9bbed80f-da6f-43e6-942a-1386c06bdff3)

Company: https://www.keypedia.com/companies/lumendi-llc/488a85d4-45e4-4d10-80b8-0a2bf400aa4b

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