# FDA Inspection 1255164 - Lujena, Inc - November 19, 2024

Source: https://www.keypedia.com/records/fda_inspections/lujena-inc/bbaffe51-c324-465f-ba5b-d849fbb000ce
Source feed: FDA_Inspections

> FDA Inspection 1255164 for Lujena, Inc on November 19, 2024. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1255164
- Company Name: Lujena, Inc
- Inspection Date: 2024-11-19
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1255164 - 2024-11-19](https://www.keypedia.com/records/fda_inspections/lujena-inc/258cefed-cf9b-4fa9-8e14-19f5fa967d2e)
- [FDA Inspection 1255164 - 2024-11-19](https://www.keypedia.com/records/fda_inspections/lujena-inc/827173d5-ce93-4d84-8646-affc2f5c91b0)
- [FDA Inspection 1255164 - 2024-11-19](https://www.keypedia.com/records/fda_inspections/lujena-inc/c40729c0-ab0f-4733-915b-4e07d72fbb03)

Company: https://www.keypedia.com/companies/lujena-inc/1a30bdd6-7c5d-4744-9b82-1b88cda6e1c1

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