FDA inspection
Bright Innovation Labs: FDA inspection ending Sep 16, 2015
FDA inspection 942919 · Voluntary Action Indicated (VAI) · Santa Clarita, CA
Key facts
| Inspection ID | 942919 |
|---|---|
| Firm | Bright Innovation Labs |
| FEI number | 1000125317 |
| Address | 26455 Ruether Ave |
| City | Santa Clarita |
| State | CA |
| ZIP | 91350 |
| Country | United States |
| Fiscal year | 2015 |
| Inspection end date | Sep 16, 2015 |
| 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