FDA inspection
Hospira Worldwide, LLC: FDA inspection ending Jan 29, 2019
FDA inspection 1080179 · No Action Indicated (NAI) · Pleasant Prairie, WI
Key facts
| Inspection ID | 1080179 |
|---|---|
| Firm | Hospira Worldwide, LLC |
| FEI number | 3005564767 |
| Address | 10501 80th Ave |
| City | Pleasant Prairie |
| State | WI |
| ZIP | 53158 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Jan 29, 2019 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No Form FDA 483 issued
- No Establishment inspection report (EIR) exists
- 10–99 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