ILMO Products Company
FDA inspection history in Jacksonville, Illinois, 2024
- 1
- Form 483
Every document, by year
- Form 483
2024: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2024One Form 483, at Jacksonville, Illinois.
Cited most
Across all ILMO Products observations on file
- 21 CFR 211.100Written procedures; deviations1
- 21 CFR 211.125Labeling issuance1
- 21 CFR 211.160General requirements1
- 21 CFR 211.180General requirements1
- 21 CFR 211.22Responsibilities of quality control unit1
The complete ILMO Products file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Jacksonville, Illinois
One Form 483 · 2024 · 6 observations
Latest: Form 483, Mar 28, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-03-28 | 483 Form 483 | Jacksonville, Illinois | 6 | $99 |
Investigators on these documents
FEI number 1454831 · most recent document Mar 28, 2024
About ILMO Products Company
How many FDA Form 483s has ILMO Products Company received?
FDA Intel has 1 Form 483 on file for ILMO Products Company; the most recent is dated Mar 28, 2024.
When was ILMO Products Company last inspected by FDA?
The most recent FDA inspection document on file for ILMO Products Company is a Form 483 dated Mar 28, 2024, for the site in Jacksonville, Illinois.
What did FDA cite at ILMO Products Company?
The regulations cited most in the observations on file for ILMO Products Company are 21 CFR 211.100 (Written procedures; deviations), 1 time; 21 CFR 211.125 (Labeling issuance), 1 time; 21 CFR 211.160 (General requirements), 1 time.