FDA inspection
Primus Sterilizer Co Inc: FDA inspection ending Jan 28, 2015
FDA inspection 914385 · No Action Indicated (NAI) · Great Bend, KS
Key facts
| Inspection ID | 914385 |
|---|---|
| Firm | Primus Sterilizer Co Inc |
| FEI number | 1000119270 |
| Address | 3707 Main St |
| City | Great Bend |
| State | KS |
| ZIP | 67530 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Jan 28, 2015 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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