FDA inspection
In VitroTech Labs, Inc.: FDA inspection ending Aug 16, 2012
FDA inspection 796648 · No Action Indicated (NAI) · West Hollywood, CA
Key facts
| Inspection ID | 796648 |
|---|---|
| Firm | In VitroTech Labs, Inc. |
| FEI number | 3008771840 |
| Address | 9201 W Sunset Blvd Ste 202 |
| City | West Hollywood |
| State | CA |
| ZIP | 90069 |
| Country | United States |
| Fiscal year | 2012 |
| Inspection end date | Aug 16, 2012 |
| Classification | No Action Indicated (NAI) |
| Project area | Human Cellular, Tissue, and Gene Therapies |
| Product type | Biologics |
At a glance
- None Citations
- None Posted citations
- No Warning letter followed
- No 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