FDA inspection
Devices & Services Co: FDA inspection ending May 5, 2005
FDA inspection 379605 · Voluntary Action Indicated (VAI) · Dallas, TX
Key facts
| Inspection ID | 379605 |
|---|---|
| Firm | Devices & Services Co |
| FEI number | 1643795 |
| Address | 10290 Monroe Dr Ste 202 |
| City | Dallas |
| State | TX |
| ZIP | 75229-5741 |
| Fiscal year | 2005 |
| Inspection end date | May 5, 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