# FDA Inspection 1250110 - Newman Medical - September 25, 2024

Source: https://www.globalkeysolutions.net/records/fda_inspections/newman-medical/8b6914ca-2f3e-43d5-bfbb-d676e1d18939
Source feed: FDA_Inspections

> FDA Inspection 1250110 for Newman Medical on September 25, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1250110
- Company Name: Newman Medical
- Inspection Date: 2024-09-25
- 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 1250110 - 2024-09-25](https://www.globalkeysolutions.net/records/fda_inspections/newman-medical/e9295a54-6dcb-47cd-b520-86eafc2531ac)
- [FDA Inspection 1250110 - 2024-09-25](https://www.globalkeysolutions.net/records/fda_inspections/newman-medical/5ddcdd3c-d1f9-44fd-b9c5-f547a0dcd580)
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- [FDA Inspection 1091306 - 2019-05-31](https://www.globalkeysolutions.net/records/fda_inspections/newman-medical/6fec244f-83f3-47a8-8a86-708ced54c59a)

Company: https://www.globalkeysolutions.net/companies/newman-medical/9ccbc85f-9be9-443e-850f-c5d99d5eefa6

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