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

Source: https://www.keypedia.com/records/fda_inspections/neosoma-inc/64beab2a-c5ae-4251-9609-d836163d2e90
Source feed: FDA_Inspections

> FDA Inspection 1262847 for Neosoma, Inc. on February 21, 2025. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 1262847
- Company Name: Neosoma, Inc.
- Inspection Date: 2025-02-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: New England District Office

## Related Documents

- [FDA Inspection 1262847 - 2025-02-21](https://www.keypedia.com/records/fda_inspections/neosoma-inc/03d9ccfd-bfc3-4331-a95a-c9af0b42505a)
- [FDA Inspection 1262847 - 2025-02-21](https://www.keypedia.com/records/fda_inspections/neosoma-inc/4637b338-7a85-4939-bbac-2d7546cb0284)
- [FDA Inspection 1262847 - 2025-02-21](https://www.keypedia.com/records/fda_inspections/neosoma-inc/105c50a3-8e43-45dd-8801-65553f8f96de)

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

Office: https://www.keypedia.com/offices/new-england-district-office/aa458072-2f1d-4231-89f5-21ba7a3b7144