FDA inspection
Deka Research & Development Corp.: FDA inspection ending Jul 1, 2003
FDA inspection 282021 · No Action Indicated (NAI) · Manchester, NH
Key facts
| Inspection ID | 282021 |
|---|---|
| Firm | Deka Research & Development Corp. |
| FEI number | 1220973 |
| Address | 340 Commercial St Fl 4 |
| City | Manchester |
| State | NH |
| ZIP | 03101-1121 |
| Fiscal year | 2003 |
| Inspection end date | Jul 1, 2003 |
| 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