# FDA Inspection 1232426 - NeoMedlight - March 07, 2024

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

> FDA Inspection 1232426 for NeoMedlight on March 07, 2024. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1232426 - 2024-03-07](https://www.keypedia.com/records/fda_inspections/neomedlight/0c00168b-58b8-4c57-8c06-6fc38607f97b)

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