Burton Medical
FDA inspection history in Addison, Illinois, 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 Addison, Illinois.
Cited most
Across all Burton Medical observations on file
- 21 CFR 830.300(a)Devices subject to device identification data submission requirements1
The complete Burton Medical file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Addison, Illinois
One Form 483 · 2026 · 1 observation
Latest: Form 483, Feb 20, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-02-20 | 483 Form 483 | Addison, Illinois | 1 | $99 |
Investigators on these documents
FEI number 3009542956 · most recent document Feb 20, 2026
About Burton Medical
How many FDA Form 483s has Burton Medical received?
FDA Intel has 1 Form 483 on file for Burton Medical; the most recent is dated Feb 20, 2026.
When was Burton Medical last inspected by FDA?
The most recent FDA inspection document on file for Burton Medical is a Form 483 dated Feb 20, 2026, for the site in Addison, Illinois.
What did FDA cite at Burton Medical?
The regulations cited most in the observations on file for Burton Medical are 21 CFR 830.300(a) (Devices subject to device identification data submission requirements), 1 time.