FDA inspection
New Standard Device Inc: FDA inspection ending Aug 20, 2021
FDA inspection 1153856 · Voluntary Action Indicated (VAI) · San Antonio, TX
Key facts
| Inspection ID | 1153856 |
|---|---|
| Firm | New Standard Device Inc |
| FEI number | 3015536247 |
| Address | 4848 Research Dr |
| City | San Antonio |
| State | TX |
| ZIP | 78240-5005 |
| Fiscal year | 2021 |
| Inspection end date | Aug 20, 2021 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Medical 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