FDA inspection
Drug Detection Devices, Ltd.: FDA inspection ending Nov 30, 1999
FDA inspection 4951 · No Action Indicated (NAI) · Alpharetta, GA
Key facts
| Inspection ID | 4951 |
|---|---|
| Firm | Drug Detection Devices, Ltd. |
| FEI number | 3002865981 |
| Address | 6820 Meadowridge Ct Ste A7 |
| City | Alpharetta |
| State | GA |
| ZIP | 30005-2252 |
| Fiscal year | 2000 |
| Inspection end date | Nov 30, 1999 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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