Overview
- 4 FDA inspections are on record.
- 2 inspections produced a Form 483.
- The most recent recorded inspection date is 2023-08-04.
At a glance
Inspections
4
Form 483s
2
EIRs
1
Last outcome
Form 483
Inspection history
FDA inspections on record, most recent first.
| Inspection | Category | Outcome | Form 483 |
|---|---|---|---|
| 31 Jul 2023 – 4 Aug 2023 | Human Drugs | 483 | On file |
| 11 Dec 2017 – 15 Dec 2017 | Human Drugs | Clean | |
| 30 Nov 2015 – 4 Dec 2015 | Human Drugs | 483 | On file |
| 19 Oct 2012 | Not recorded | Clean |
Investigators
FDA investigators tied to this site in the record.
Claudia M Perez-Kasmarski1 insp.
Muna Algharibeh1 insp.
Reba A Gates1 insp.
Rafael Nevarez Nieves1 insp.
Ana P Pineda Zavaleta1 insp.
German Rivera1 insp.
Heriberto Negron-Rivera1 insp.
Full site report
Get the verbatim findings behind Laboratorios Liomont, S.A. de C.V.'s 2 Form 483s
The full inspection record, as Atlas holds it, so your team knows what this site gets cited for.
- The site's full inspection history, with every Form 483 and its outcome
- Warning letters and recalls tied to the company behind it
- Whether recurring CFR citations get closed out or repeat