LEO Laboratories Ltd.
FDA inspection history in Crumlin, Ireland, 2022
- 1
- Form 483
Every document, by year
- Form 483
2022: one Form 483.
The story so far
Built from the dates and citations on the documents themselves.
- 2022One Form 483, at Crumlin, Ireland.
Cited most
Across all LEO Laboratories observations on file
- 21 CFR 211.46(b)Ventilation, air filtration, air heating and cooling1
- 21 CFR 211.48(a)Plumbing1
The complete LEO Laboratories file.
All 1 documents as original PDFs. For supplier audits, diligence and inspection prep.
Sites
Crumlin, Ireland
One Form 483 · 2022 · 2 observations
Latest: Form 483, Jun 24, 2022 →
Documents
1 on file, newest first| Date | Document | Location | Observations | Price |
|---|---|---|---|---|
| 2022-06-24 | 483 Form 483 | Crumlin, Ireland | 2 | $99 |
FEI number 3002807468 · most recent document Jun 24, 2022
About LEO Laboratories Ltd.
How many FDA Form 483s has LEO Laboratories Ltd. received?
FDA Intel has 1 Form 483 on file for LEO Laboratories Ltd.; the most recent is dated Jun 24, 2022.
When was LEO Laboratories Ltd. last inspected by FDA?
The most recent FDA inspection document on file for LEO Laboratories Ltd. is a Form 483 dated Jun 24, 2022, for the site in Crumlin, Ireland.
What did FDA cite at LEO Laboratories Ltd.?
The regulations cited most in the observations on file for LEO Laboratories Ltd. are 21 CFR 211.46(b) (Ventilation, air filtration, air heating and cooling), 1 time; 21 CFR 211.48(a) (Plumbing), 1 time.