Brius Technologies Inc
FDA inspection history in Carrollton, Texas, 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 Carrollton, Texas.
Cited most
Across all Brius Technologies observations on file
- 21 CFR 803.50(a)(1)If I am a manufacturer, what reporting requirements apply to me?1
- 21 CFR 820.100(b)Corrective and preventive action1
- 21 CFR 820.198(c)Complaint files1
- 21 CFR 820.72(a)Inspection, measuring, and test equipment1
- 21 CFR 820.90(a)Nonconforming product1
The complete Brius Technologies file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Carrollton, Texas
One Form 483 · 2024 · 5 observations
Latest: Form 483, Oct 7, 2024 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2024-10-07 | 483 Form 483 | Carrollton, Texas | 5 | $99 |
Investigators on these documents
FEI number 3014680924 · most recent document Oct 7, 2024
About Brius Technologies Inc
How many FDA Form 483s has Brius Technologies Inc received?
FDA Intel has 1 Form 483 on file for Brius Technologies Inc; the most recent is dated Oct 7, 2024.
When was Brius Technologies Inc last inspected by FDA?
The most recent FDA inspection document on file for Brius Technologies Inc is a Form 483 dated Oct 7, 2024, for the site in Carrollton, Texas.
What did FDA cite at Brius Technologies Inc?
The regulations cited most in the observations on file for Brius Technologies Inc are 21 CFR 803.50(a)(1) (If I am a manufacturer, what reporting requirements apply to me?), 1 time; 21 CFR 820.100(b) (Corrective and preventive action), 1 time; 21 CFR 820.198(c) (Complaint files), 1 time.