FDA inspection
Stericycle Inc: FDA inspection ending Feb 21, 2018
FDA inspection 1041855 · Voluntary Action Indicated (VAI) · Aurora, IL
Key facts
| Inspection ID | 1041855 |
|---|---|
| Firm | Stericycle Inc |
| FEI number | 3012237654 |
| Address | 3557 Butterfield Rd Ste 151 |
| City | Aurora |
| State | IL |
| ZIP | 60502 |
| Country | United States |
| Fiscal year | 2018 |
| Inspection end date | Feb 21, 2018 |
| 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