FDA inspection
Steritec Products Mfg. Co., Inc.: FDA inspection ending May 10, 2005
FDA inspection 379592 · Englewood, CO
Key facts
| Inspection ID | 379592 |
|---|---|
| Firm | Steritec Products Mfg. Co., Inc. |
| FEI number | 1000125215 |
| Address | 74 Inverness Dr E |
| City | Englewood |
| State | CO |
| ZIP | 80112-5114 |
| Fiscal year | 2005 |
| Inspection end date | May 10, 2005 |
| 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