FDA inspection
Diabetes Sentry Products: FDA inspection ending Apr 1, 2003
FDA inspection 267970 · No Action Indicated (NAI) · Fort Worth, TX
Key facts
| Inspection ID | 267970 |
|---|---|
| Firm | Diabetes Sentry Products |
| FEI number | 3003636198 |
| Address | 501 Samuels Ave Apt 110 |
| City | Fort Worth |
| State | TX |
| ZIP | 76102-8641 |
| Fiscal year | 2003 |
| Inspection end date | Apr 1, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Product Evaluation: 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