FDA inspection
THEROZONE USA, INC.: FDA inspection ending May 31, 2012
FDA inspection 784308 · Voluntary Action Indicated (VAI) · Santa Monica, CA
Key facts
| Inspection ID | 784308 |
|---|---|
| Firm | THEROZONE USA, INC. |
| FEI number | 3007025733 |
| Address | 2701 Ocean Park Blvd Ste 108 |
| City | Santa Monica |
| State | CA |
| ZIP | 90405 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | May 31, 2012 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Compliance: 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