FDA inspection
Hospira, Inc.: FDA inspection ending Nov 15, 2013
FDA inspection 855618 · Official Action Indicated (OAI) · Rocky Mount, NC
Key facts
| Inspection ID | 855618 |
|---|---|
| Firm | Hospira, Inc. |
| FEI number | 1021343 |
| Address | Highway 301 North |
| City | Rocky Mount |
| State | NC |
| ZIP | 27801 |
| Country | United States |
| Fiscal year | 2014 |
| Inspection end date | Nov 15, 2013 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
| Warning letter | 422589 |
At a glance
- None Citations
- 1–9 Posted citations
- Yes Warning letter followed
- Yes 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