Nuclein LLC
FDA inspection history in Austin, 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 Austin, Texas.
Cited most
Across all Nuclein observations on file
- 21 CFR 820.198(c)Complaint files1
- 21 CFR 820.250(b)Statistical techniques1
- 21 CFR 820.30(g)Design controls1
The complete Nuclein file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Austin, Texas
One Form 483 · 2026 · 3 observations
Latest: Form 483, Jan 13, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-01-13 | 483 Form 483 | Austin, Texas | 3 | $99 |
Investigators on these documents
FEI number 3014515702 · most recent document Jan 13, 2026
About Nuclein LLC
How many FDA Form 483s has Nuclein LLC received?
FDA Intel has 1 Form 483 on file for Nuclein LLC; the most recent is dated Jan 13, 2026.
When was Nuclein LLC last inspected by FDA?
The most recent FDA inspection document on file for Nuclein LLC is a Form 483 dated Jan 13, 2026, for the site in Austin, Texas.
What did FDA cite at Nuclein LLC?
The regulations cited most in the observations on file for Nuclein LLC are 21 CFR 820.198(c) (Complaint files), 1 time; 21 CFR 820.250(b) (Statistical techniques), 1 time; 21 CFR 820.30(g) (Design controls), 1 time.