FDA inspection
Laboratorios Liomont, S.A. de C.V.: FDA inspection ending Oct 19, 2012
FDA inspection 808251 · No Action Indicated (NAI) · Ciudad De Mexico
Key facts
| Inspection ID | 808251 |
|---|---|
| Firm | Laboratorios Liomont, S.A. de C.V. |
| FEI number | 3003948827 |
| Address | Calle Adolfo Lopez Mateos No. 68, Col. Cuajimalpa, Cuajimalpa De Morelos |
| City | Ciudad De Mexico |
| Country | Mexico |
| Fiscal year | 2013 |
| Inspection end date | Oct 19, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 1–9 Inspections at this FEI
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA inspections
FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.
Source: U.S. Food and Drug Administration (FDA), inspection classification data