Tristel Solutions Limited
FDA inspection history on file, 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.
Cited most
Across all Tristel Solutions Limited observations on file
- 21 CFR 820.100(a)Corrective and preventive action1
- 21 CFR 820.30(g)Design controls1
- 21 CFR 820.90(a)Nonconforming product1
The complete Tristel Solutions Limited file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-02-13 | 483 Form 483 | — | 3 | $99 |
Investigators on these documents
FEI number 3006892175 · most recent document Feb 13, 2025
About Tristel Solutions Limited
How many FDA Form 483s has Tristel Solutions Limited received?
FDA Intel has 1 Form 483 on file for Tristel Solutions Limited; the most recent is dated Feb 13, 2025.
When was Tristel Solutions Limited last inspected by FDA?
The most recent FDA inspection document on file for Tristel Solutions Limited is a Form 483 dated Feb 13, 2025.
What did FDA cite at Tristel Solutions Limited?
The regulations cited most in the observations on file for Tristel Solutions Limited are 21 CFR 820.100(a) (Corrective and preventive action), 1 time; 21 CFR 820.30(g) (Design controls), 1 time; 21 CFR 820.90(a) (Nonconforming product), 1 time.