FDA inspection
ERIKA DE REYNOSA, S.A. DE C.V.: FDA inspection ending Aug 10, 2017
FDA inspection 1052933 · No Action Indicated (NAI) · Reynosa
Key facts
| Inspection ID | 1052933 |
|---|---|
| Firm | ERIKA DE REYNOSA, S.A. DE C.V. |
| FEI number | 3002807744 |
| Address | Mike Allen 1331, Zona Industrial Parque Industrial Center, Reynosa |
| City | Reynosa |
| Fiscal year | 2017 |
| Inspection end date | Aug 10, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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