FDA inspection
Abbott Molecular, Inc.: FDA inspection ending Jul 11, 2012
FDA inspection 790935 · Voluntary Action Indicated (VAI) · Des Plaines, IL
Key facts
| Inspection ID | 790935 |
|---|---|
| Firm | Abbott Molecular, Inc. |
| FEI number | 3005248192 |
| Address | 1300 E Touhy Ave |
| City | Des Plaines |
| State | IL |
| ZIP | 60018 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Jul 11, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: Devices |
| Product type | Devices |
At a glance
- 1–9 Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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