FDA inspection
Advanced Sterilization Products: FDA inspection ending Aug 11, 2017
FDA inspection 1034571 · No Action Indicated (NAI) · Irvine, CA
Key facts
| Inspection ID | 1034571 |
|---|---|
| Firm | Advanced Sterilization Products |
| FEI number | 3003662624 |
| Address | 33 Technology Dr |
| City | Irvine |
| State | CA |
| ZIP | 92618-2346 |
| Fiscal year | 2017 |
| Inspection end date | Aug 11, 2017 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Medical Devices |
| Product type | Devices |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes 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