PETNET Solutions, Inc.
FDA inspection history in Las Vegas, Nevada, 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 Las Vegas, Nevada.
Cited most
Across all PETNET Solutions observations on file
- 21 CFR 212.20(e)What activities must I perform to ensure drug quality?1
- 21 CFR 212.50What production and process controls must I have?1
The complete PETNET Solutions file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Las Vegas, Nevada
One Form 483 · 2026 · 2 observations
Latest: Form 483, Mar 6, 2026 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2026-03-06 | 483 Form 483 | Las Vegas, Nevada | 2 | $99 |
Investigators on these documents
FEI number 3009856092 · most recent document Mar 6, 2026
About PETNET Solutions, Inc.
How many FDA Form 483s has PETNET Solutions, Inc. received?
FDA Intel has 1 Form 483 on file for PETNET Solutions, Inc.; the most recent is dated Mar 6, 2026.
When was PETNET Solutions, Inc. last inspected by FDA?
The most recent FDA inspection document on file for PETNET Solutions, Inc. is a Form 483 dated Mar 6, 2026, for the site in Las Vegas, Nevada.
What did FDA cite at PETNET Solutions, Inc.?
The regulations cited most in the observations on file for PETNET Solutions, Inc. are 21 CFR 212.20(e) (What activities must I perform to ensure drug quality?), 1 time; 21 CFR 212.50 (What production and process controls must I have?), 1 time.