FDA inspection
Exel International Co.: FDA inspection ending Aug 28, 2000
FDA inspection 40731 · No Action Indicated (NAI) · Redondo Beach, CA
Key facts
| Inspection ID | 40731 |
|---|---|
| Firm | Exel International Co. |
| FEI number | 1035907 |
| Address | 2500 Santa Fe Ave |
| City | Redondo Beach |
| State | CA |
| ZIP | 90278-1116 |
| Fiscal year | 2000 |
| Inspection end date | Aug 28, 2000 |
| Classification | No Action Indicated (NAI) |
| Project area | Compliance: Med Devices |
| 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