FDA inspection
Positron Corporation: FDA inspection ending Mar 24, 2005
FDA inspection 372121 · Voluntary Action Indicated (VAI) · Houston, TX
Key facts
| Inspection ID | 372121 |
|---|---|
| Firm | Positron Corporation |
| FEI number | 1640378 |
| Address | 1304 Langham Creek Dr Ste 300 |
| City | Houston |
| State | TX |
| ZIP | 77084-5043 |
| Fiscal year | 2005 |
| Inspection end date | Mar 24, 2005 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- 1–9 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