# FDA Inspection 1255815 - Mezlight LLC - November 21, 2024

Source: https://www.keypedia.com/records/fda_inspections/mezlight-llc/bad056e1-cbc7-4e4f-95e0-559a8860aaf8
Source feed: FDA_Inspections

> FDA Inspection 1255815 for Mezlight LLC on November 21, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1255815
- Company Name: Mezlight LLC
- Inspection Date: 2024-11-21
- 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 1255815 - 2024-11-21](https://www.keypedia.com/records/fda_inspections/mezlight-llc/f9ae12d4-52da-4618-8f77-3a44dbfbb8cd)
- [FDA Inspection 1255815 - 2024-11-21](https://www.keypedia.com/records/fda_inspections/mezlight-llc/a948dd39-be55-4670-8708-658e005b9209)

Company: https://www.keypedia.com/companies/mezlight-llc/920bab02-66fc-432f-b009-a95943a84596

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