ICON PLC
FDA inspection history in Lenexa, Kansas, 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, at Lenexa, Kansas.
Cited most
Across all ICON observations on file
- 21 CFR 320.29Analytical methods for an in vivo bioavailability or bioequivalence study1
The complete ICON file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Lenexa, Kansas
One Form 483 · 2025 · 3 observations
Latest: Form 483, Jun 13, 2025 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2025-06-13 | 483 Form 483 | Lenexa, Kansas | 3 | $99 |
Investigators on these documents
FEI number 3020784373 · most recent document Jun 13, 2025
About ICON PLC
How many FDA Form 483s has ICON PLC received?
FDA Intel has 1 Form 483 on file for ICON PLC; the most recent is dated Jun 13, 2025.
When was ICON PLC last inspected by FDA?
The most recent FDA inspection document on file for ICON PLC is a Form 483 dated Jun 13, 2025, for the site in Lenexa, Kansas.
What did FDA cite at ICON PLC?
The regulations cited most in the observations on file for ICON PLC are 21 CFR 320.29 (Analytical methods for an in vivo bioavailability or bioequivalence study), 1 time.