Marson Medical, Inc.
E-64 MIDLAND AVE., PARAMUS, NJ, US
Registered product codes
12 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 1000550978.
FDA inspections
2 on file
- Official Action Indicated (OAI)Jan 16, 2026
Compliance: Devices · Citations posted
- No Action Indicated (NAI)Jan 16, 2026
Postmarket Assurance: Devices · Citations posted
Inspection citations
11 on file
Top cited requirements
Compare to industry ↗21 CFR 820.22Quality audits - auditor independence
121 CFR 820.25(b)Training - Lack of or inadequate procedures
121 CFR 820.40Procedures not adequately established or maintained
121 CFR 820.70(a)Process control procedures, Lack of or inadequate procedures
121 CFR 820.75(a)Lack of or inadequate process validation
121 CFR 820.75(b)Lack/Inad procedure-Monitoring/Control of Validated Proces
1
- 21 CFR 820.22Jan 16, 2026
Quality audits - auditor independence
- 21 CFR 820.25(b)Jan 16, 2026
Training - Lack of or inadequate procedures
- 21 CFR 820.40Jan 16, 2026
Procedures not adequately established or maintained
- 21 CFR 820.70(a)Jan 16, 2026
Process control procedures, Lack of or inadequate procedures
- 21 CFR 820.75(a)Jan 16, 2026
Lack of or inadequate process validation
- 21 CFR 820.75(b)Jan 16, 2026
Lack/Inad procedure-Monitoring/Control of Validated Proces
- 21 CFR 820.90(a)Jan 16, 2026
Nonconforming product, Lack of or inadequate procedures
- 21 CFR 820.100(a)Jan 16, 2026
Lack of or inadequate procedures
- 21 CFR 820.184Jan 16, 2026
Lack of or inadequate DHR procedures
- 21 CFR 820.198(a)Jan 16, 2026
Lack of or inadequate complaint procedures
- 21 CFR 820.250(b)Jan 16, 2026
Sampling plans
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.