FDA inspection
Primus Sterilizer Co Inc: FDA inspection ending Feb 21, 2017
FDA inspection 1003248 · Voluntary Action Indicated (VAI) · Great Bend, KS
Key facts
| Inspection ID | 1003248 |
|---|---|
| Firm | Primus Sterilizer Co Inc |
| FEI number | 1000119270 |
| Address | 8719 S 135th St Ste 300 |
| City | Great Bend |
| State | KS |
| ZIP | 67530 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Feb 21, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Postmarket Assurance: 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
- 10–99 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