FDA inspection
Products By O2, Inc: FDA inspection ending Mar 16, 2017
FDA inspection 1005899 · Voluntary Action Indicated (VAI) · Fort Lauderdale, FL
Key facts
| Inspection ID | 1005899 |
|---|---|
| Firm | Products By O2, Inc |
| FEI number | 3005835723 |
| Address | 3020 High Ridge Rd Ste 300 |
| City | Fort Lauderdale |
| State | FL |
| ZIP | 33309 |
| Country | United States |
| Fiscal year | 2017 |
| Inspection end date | Mar 16, 2017 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Drug Quality Assurance |
| Product type | Drugs |
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