FDA inspection
O-Two Medical Technologies, Inc.: FDA inspection ending Oct 31, 2001
FDA inspection 209975 · Voluntary Action Indicated (VAI) · Brampton
Key facts
| Inspection ID | 209975 |
|---|---|
| Firm | O-Two Medical Technologies, Inc. |
| FEI number | 3002807836 |
| Address | 45A Armthorpe Road |
| City | Brampton |
| Fiscal year | 2002 |
| Inspection end date | Oct 31, 2001 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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