FDA inspection
PDM Acondifarma, S.A. de C.V.: FDA inspection ending Dec 2, 2016
FDA inspection 1006378 · Voluntary Action Indicated (VAI) · Ramos Arizpe
Key facts
| Inspection ID | 1006378 |
|---|---|
| Firm | PDM Acondifarma, S.A. de C.V. |
| FEI number | 3002815808 |
| Address | Calle Industria Automotriz No. 3089, Col. Zona Industrial, Ramos Arizpe |
| City | Ramos Arizpe |
| Country | Mexico |
| Fiscal year | 2017 |
| Inspection end date | Dec 2, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
At a glance
- 1–9 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