FDA inspection
Hemostatix Medical Technologies LLC: FDA inspection ending Oct 17, 2007
FDA inspection 501254 · No Action Indicated (NAI) · Bartlett, TN
Key facts
| Inspection ID | 501254 |
|---|---|
| Firm | Hemostatix Medical Technologies LLC |
| FEI number | 3006119098 |
| Address | 8400 Wolf Lake Dr Ste 109 |
| City | Bartlett |
| State | TN |
| ZIP | 38133-4189 |
| Fiscal year | 2008 |
| Inspection end date | Oct 17, 2007 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| Product type | Devices |
At a glance
- None Citations
- None 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