FDA inspection
Oxyhealth, LLC: FDA inspection ending Dec 13, 2000
FDA inspection 58230 · Voluntary Action Indicated (VAI) · Santa Fe Springs, CA
Key facts
| Inspection ID | 58230 |
|---|---|
| Firm | Oxyhealth, LLC |
| FEI number | 3006777109 |
| Address | 10719 Norwalk Blvd |
| City | Santa Fe Springs |
| State | CA |
| ZIP | 90670-3823 |
| Fiscal year | 2001 |
| Inspection end date | Dec 13, 2000 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Med Devices |
| 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