FDA inspection
MaineHealth IRB #1: FDA inspection ending Jun 26, 2001
FDA inspection 80668 · Official Action Indicated (OAI) · Portland, ME
Key facts
| Inspection ID | 80668 |
|---|---|
| Firm | MaineHealth IRB #1 |
| FEI number | 3003354649 |
| Address | 509 Forest Ave Ste 350 |
| City | Portland |
| State | ME |
| ZIP | 04101-1521 |
| Fiscal year | 2001 |
| Inspection end date | Jun 26, 2001 |
| Classification | Official Action Indicated (OAI) |
| Project area | Product Evaluation: Med 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