FDA inspection
Nuline Sensors LLC: FDA inspection ending Jan 29, 2016
FDA inspection 969793 · Voluntary Action Indicated (VAI) · Sanford, FL
Key facts
| Inspection ID | 969793 |
|---|---|
| Firm | Nuline Sensors LLC |
| FEI number | 3010666140 |
| Address | 210 Specialty Pt |
| City | Sanford |
| State | FL |
| ZIP | 32771 |
| Country | United States |
| Fiscal year | 2016 |
| Inspection end date | Jan 29, 2016 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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