FDA inspection
Kree Technologies USA Inc: FDA inspection ending Feb 25, 2000
FDA inspection 14816 · Voluntary Action Indicated (VAI) · Clearwater, FL
Key facts
| Inspection ID | 14816 |
|---|---|
| Firm | Kree Technologies USA Inc |
| FEI number | 3002732542 |
| Address | 11429 53rd Street North |
| City | Clearwater |
| State | FL |
| ZIP | 33760-4824 |
| Fiscal year | 2000 |
| Inspection end date | Feb 25, 2000 |
| 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