FDA inspection
Advarra IRB: FDA inspection ending Jul 28, 2000
FDA inspection 32108 · No Action Indicated (NAI) · Columbia, MD
Key facts
| Inspection ID | 32108 |
|---|---|
| Firm | Advarra IRB |
| FEI number | 3002908905 |
| Address | 6100 Merriweather Dr, Ste 600 |
| City | Columbia |
| State | MD |
| ZIP | 21044 |
| Fiscal year | 2000 |
| Inspection end date | Jul 28, 2000 |
| 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
- 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