Aurorium LLC
FDA inspection history in Midlothian, Texas, 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 Midlothian, Texas.
Cited most
Across all Aurorium observations on file
- 21 CFR 211.160General requirements1
- 21 CFR 211.180General requirements1
- 21 CFR 211.192Production record review1
- 21 CFR 211.22Responsibilities of quality control unit1
- 21 CFR 211.58Maintenance1
The complete Aurorium file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Midlothian, Texas
One Form 483 · 2026 · 5 observations
Latest: Form 483, Mar 6, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-06 | 483 Form 483 | Midlothian, Texas | 5 | $99 |
Investigators on these documents
FEI number 1628757 · most recent document Mar 6, 2026
About Aurorium LLC
How many FDA Form 483s has Aurorium LLC received?
FDA Intel has 1 Form 483 on file for Aurorium LLC; the most recent is dated Mar 6, 2026.
When was Aurorium LLC last inspected by FDA?
The most recent FDA inspection document on file for Aurorium LLC is a Form 483 dated Mar 6, 2026, for the site in Midlothian, Texas.
What did FDA cite at Aurorium LLC?
The regulations cited most in the observations on file for Aurorium LLC are 21 CFR 211.160 (General requirements), 1 time; 21 CFR 211.180 (General requirements), 1 time; 21 CFR 211.192 (Production record review), 1 time.