Neosoma, Inc. – FDA Inspection, Feb 21, 2025

Record Details

This FDA Inspection record concerns Neosoma, Inc., with an inspection on February 21, 2025, issued by the New England District Office, covering medical devices & rad health.

Company: Neosoma, Inc.
Inspection Date: February 21, 2025
Product Type: Medical Devices & Rad Health
Office: New England District Office
Person: Nabil Nakhoul (Issuing Officer)

View Company Profile

ID · 64beab2a-c5ae-4251-9609-d836163d2e90

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number: 1262847
FDA center: Medical Devices & Rad Health
Project area: Postmarket Assurance: Medical Devices
Outcome: Form 483 issued, view the record

FDA Citations

21 CFR 820.184DHR - not or inadequately maintained
21 CFR 820.181DMR - not or inadequately maintained
21 CFR 820.90(b)(1)Procedures for product review,disposition lack of/inadequate

Full citation text and observation details available on the Dashboard.

Discuss this record with AI

KeyPedia

ChatGPT

Claude

Perplexity

Grok

Copilot

Document or profile

One record shows the event. A profile shows the pattern.

Buy this document for the source file and details behind this single event.

Choose full profile access to connect related records, sites, people, citations, and enforcement history in one view.

Explore Neosoma, Inc.

FDA Inspection

Neosoma, Inc.February 21, 2025