FDA inspection
Masterile Reprocessing, Inc.: FDA inspection ending Sep 30, 2000
FDA inspection 55220 · Warrenville, IL
Key facts
| Inspection ID | 55220 |
|---|---|
| Firm | Masterile Reprocessing, Inc. |
| FEI number | 1000143874 |
| Address | 30w110 Butterfield Rd |
| City | Warrenville |
| State | IL |
| ZIP | 60555-1563 |
| Fiscal year | 2000 |
| Inspection end date | Sep 30, 2000 |
| Product type | Devices |
At a glance
- None Citations
- None 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