FDA inspection
Hospira Costa Rica Ltda: FDA inspection ending Jul 23, 2003
FDA inspection 289980 · No Action Indicated (NAI) · Heredia
Key facts
| Inspection ID | 289980 |
|---|---|
| Firm | Hospira Costa Rica Ltda |
| FEI number | 3002999813 |
| Address | La Aurora De Heredia,1 Km Noreste Dplaza, Real Cariari, Global Park De Entrada 300 |
| City | Heredia |
| Fiscal year | 2003 |
| Inspection end date | Jul 23, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med 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