FDA inspection
Selgel Mexico SA de CV: FDA inspection ending Sep 15, 2017
FDA inspection 1027819 · Voluntary Action Indicated (VAI) · Toluca De Lerdo
Key facts
| Inspection ID | 1027819 |
|---|---|
| Firm | Selgel Mexico SA de CV |
| FEI number | 3011183638 |
| Address | 7 Norte No. 115, Parque Industrial Toluca 2nd Extension |
| City | Toluca De Lerdo |
| Country | Mexico |
| Fiscal year | 2017 |
| Inspection end date | Sep 15, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- No 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