FDA inspection
CellRight Technologies LLC: FDA inspection ending Mar 15, 2019
FDA inspection 1082842 · Voluntary Action Indicated (VAI) · Universal City, TX
Key facts
| Inspection ID | 1082842 |
|---|---|
| Firm | CellRight Technologies LLC |
| FEI number | 3009234552 |
| Address | 1808 Universal City Blvd |
| City | Universal City |
| State | TX |
| ZIP | 78148 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Mar 15, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Blood and Blood Products |
| Product type | Biologics |
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