FDA inspection
MECTA Corporation: FDA inspection ending Aug 2, 2011
FDA inspection 737273 · No Action Indicated (NAI) · Tualatin, OR
Key facts
| Inspection ID | 737273 |
|---|---|
| Firm | MECTA Corporation |
| FEI number | 3020533 |
| Address | 19799 Sw 95th Ave Bldg D Ste B |
| City | Tualatin |
| State | OR |
| ZIP | 97062 |
| Country | United States |
| Fiscal year | 2011 |
| Inspection end date | Aug 2, 2011 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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