FDA inspection
MAXOGEN GROUP LLC: FDA inspection ending Jun 5, 2023
FDA inspection 1207160 · Voluntary Action Indicated (VAI) · Hollywood, FL
Key facts
| Inspection ID | 1207160 |
|---|---|
| Firm | MAXOGEN GROUP LLC |
| FEI number | 3012440185 |
| Address | 2719 Hollywood Blvd Ste D10 |
| City | Hollywood |
| State | FL |
| ZIP | 33020 |
| Country | United States |
| Fiscal year | 2023 |
| Inspection end date | Jun 5, 2023 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: Devices |
| Product type | Devices |
At a glance
- 10–99 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