# FDA Inspection 1262847 - Neosoma, Inc. - February 21, 2025

Source: https://www.globalkeysolutions.net/records/fda_inspections/neosoma-inc/fb02efb8-e98e-4aaa-9f6a-a2ea02ad2013/
Source feed: FDA_Inspections

> FDA Inspection 1262847 for Neosoma, Inc. on February 21, 2025. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1262847
- Company Name: Neosoma, Inc.
- Inspection Date: 2025-02-21
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1262847 - 2025-02-21](https://www.globalkeysolutions.net/api/records/fda_inspections/neosoma-inc/d07f8808-fe93-4239-9c7d-d9d5448fd201/)
- [FDA Inspection 1262847 - 2025-02-21](https://www.globalkeysolutions.net/api/records/fda_inspections/neosoma-inc/e76b3516-90bd-4acf-94f4-376134c19b74/)
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- [FDA Inspection 1262847 - 2025-02-21](https://www.globalkeysolutions.net/api/records/fda_inspections/neosoma-inc/efcb470e-c349-46cf-b8aa-574cd6d5c42b/)

Company: https://www.globalkeysolutions.net/companies/neosoma-inc/e2d63671-b738-4af5-b2d1-072dfce312df

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