Marson Medical, Inc.
FDA inspection history in New Jersey, 2026
- 1
- Form 483
Every document, by year
- Form 483
2026: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2026One Form 483, at New Jersey.
Cited most
Across all Marson Medical observations on file
- 21 CFR 820.75(a)Process validation2
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.184Device history record1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.22Quality audit1
The complete Marson Medical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
New Jersey
One Form 483 · 2026 · 11 observations
Latest: Form 483, Jan 16, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-16 | 483 Form 483 | New Jersey | 11 | $99 |
Investigators on these documents
FEI number 1000550978 · most recent document Jan 16, 2026
About Marson Medical, Inc.
How many FDA Form 483s has Marson Medical, Inc. received?
FDA Intel has 1 Form 483 on file for Marson Medical, Inc.; the most recent is dated Jan 16, 2026.
When was Marson Medical, Inc. last inspected by FDA?
The most recent FDA inspection document on file for Marson Medical, Inc. is a Form 483 dated Jan 16, 2026, for the site in New Jersey.
What did FDA cite at Marson Medical, Inc.?
The regulations cited most in the observations on file for Marson Medical, Inc. are 21 CFR 820.75(a) (Process validation), 2 times; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.184 (Device history record), 1 time.