FDA inspection
Martech Medical Products, Mexico: FDA inspection ending Sep 28, 2017
FDA inspection 1027644 · Voluntary Action Indicated (VAI) · Mexicali
Key facts
| Inspection ID | 1027644 |
|---|---|
| Firm | Martech Medical Products, Mexico |
| FEI number | 3003915875 |
| Address | Calle Mercurio Parque Industrial 46, Parque Industrial Parque Industrial Alamo, Mexicalimexicali 1 |
| City | Mexicali |
| Country | Mexico |
| Fiscal year | 2017 |
| Inspection end date | Sep 28, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Project Evaluation: Devices |
| Product type | Devices |
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