MIDWAY MEDICAL
FDA inspection history in Bloomington, 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 Bloomington, Illinois.
Cited most
Across all MIDWAY MEDICAL observations on file
- 21 CFR 803.17What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?1
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.198(a)Complaint files1
- 21 CFR 820.50Purchasing controls1
- 21 CFR 830.300(a)Devices subject to device identification data submission requirements1
The complete MIDWAY MEDICAL file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Bloomington, Illinois
One Form 483 · 2026 · 5 observations
Latest: Form 483, Jan 15, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-15 | 483 Form 483 | Bloomington, Illinois | 5 | $99 |
Investigators on these documents
FEI number 3015536408 · most recent document Jan 15, 2026
About MIDWAY MEDICAL
How many FDA Form 483s has MIDWAY MEDICAL received?
FDA Intel has 1 Form 483 on file for MIDWAY MEDICAL; the most recent is dated Jan 15, 2026.
When was MIDWAY MEDICAL last inspected by FDA?
The most recent FDA inspection document on file for MIDWAY MEDICAL is a Form 483 dated Jan 15, 2026, for the site in Bloomington, Illinois.
What did FDA cite at MIDWAY MEDICAL?
The regulations cited most in the observations on file for MIDWAY MEDICAL are 21 CFR 803.17 (What are the requirements for developing, maintaining, and implementing written MDR procedures that apply to me?), 1 time; 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.198(a) (Complaint files), 1 time.