# NeoMedlight – FDA Inspection, Mar 7, 2024

Source: https://www.keypedia.com/records/fda_inspections/neomedlight/9b3b65f3-6f38-40a2-8fcf-5e5d67c111cb
Source feed: FDA_Inspections

> FDA inspection 1232426 of NeoMedlight, March 07, 2024. Classification: Voluntary Action Indicated (VAI). 3 citations under 21 CFR parts 803 and 820.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1232426
- Company Name: NeoMedlight
- Inspection Date: 2024-03-07
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 3

## Related Officers

- [Company Rep](https://www.keypedia.com/people/john-a-sciacchitano/9f8f49bf-1971-449e-972e-b516418ea78e)

Company: https://www.keypedia.com/companies/neomedlight/298e3fd6-0b13-4e09-b8f8-f95442fddc0f

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