Korex Chicago LLC
FDA inspection history in Chicago, Illinois, 2025
- 1
- Form 483
Every document, by year
- Form 483
2025: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2025One Form 483, at Chicago, Illinois.
Cited most
Across all Korex Chicago observations on file
- 21 CFR 211.110(a)Sampling and testing of in-process materials and drug products1
- 21 CFR 211.113(a)Control of microbiological contamination1
- 21 CFR 211.165(b)Testing and release for distribution1
- 21 CFR 211.166(a)(3)Stability testing1
- 21 CFR 211.192Production record review1
The complete Korex Chicago file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Chicago, Illinois
One Form 483 · 2025 · 6 observations
Latest: Form 483, Feb 7, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-07 | 483 Form 483 | Chicago, Illinois | 6 | $99 |
Investigators on these documents
FEI number 3006458382 · most recent document Feb 7, 2025
About Korex Chicago LLC
How many FDA Form 483s has Korex Chicago LLC received?
FDA Intel has 1 Form 483 on file for Korex Chicago LLC; the most recent is dated Feb 7, 2025.
When was Korex Chicago LLC last inspected by FDA?
The most recent FDA inspection document on file for Korex Chicago LLC is a Form 483 dated Feb 7, 2025, for the site in Chicago, Illinois.
What did FDA cite at Korex Chicago LLC?
The regulations cited most in the observations on file for Korex Chicago LLC are 21 CFR 211.110(a) (Sampling and testing of in-process materials and drug products), 1 time; 21 CFR 211.113(a) (Control of microbiological contamination), 1 time; 21 CFR 211.165(b) (Testing and release for distribution), 1 time.