FEI 3024812789
Neosoma, Inc.
44 Farmers Row, Groton, MA, US
MDR events0All time
Recalls0All time
Registered products2
Establishment typeManufactureManufacture Medical Device
Registered product codes
2 product codes
Recent MDR events
0 on file
No MDR events on file for this firm name.
Recalls
0 on file
No recalls on file for this firm name.
Compliance history
Matched by FEI 3024812789.
FDA inspections
2 on file
- Voluntary Action Indicated (VAI)Feb 21, 2025
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Feb 21, 2025
Postmarket Assurance: Devices · Citations posted
Inspection citations
3 on file
Top cited requirements
Compare to industry ↗- 21 CFR 820.90(b)(1)Feb 21, 2025
Procedures for product review,disposition lack of/inadequate
- 21 CFR 820.181Feb 21, 2025
DMR - not or inadequately maintained
- 21 CFR 820.184Feb 21, 2025
DHR - not or inadequately maintained
Compliance actions
0 on file
No warning letters or injunctions on file for this FEI number.
Import refusals
0 on file
No import refusals on file for this FEI number.