FDA inspection
Howard Instruments Inc: FDA inspection ending Sep 14, 2010
FDA inspection 681246 · Official Action Indicated (OAI) · Tuscaloosa, AL
Key facts
| Inspection ID | 681246 |
|---|---|
| Firm | Howard Instruments Inc |
| FEI number | 1039865 |
| Address | 2004 Lenox Dr |
| City | Tuscaloosa |
| State | AL |
| ZIP | 35405 |
| Country | United States |
| Fiscal year | 2010 |
| Inspection end date | Sep 14, 2010 |
| Classification | Official Action Indicated (OAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- 1–9 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