FDA inspection
Scantibodies Laboratory, Inc.: FDA inspection ending Oct 8, 2003
FDA inspection 296051 · No Action Indicated (NAI) · Santee, CA
Key facts
| Inspection ID | 296051 |
|---|---|
| Firm | Scantibodies Laboratory, Inc. |
| FEI number | 2020808 |
| Address | 9336 Abraham Way |
| City | Santee |
| State | CA |
| ZIP | 92071-2861 |
| Fiscal year | 2004 |
| Inspection end date | Oct 8, 2003 |
| Classification | No Action Indicated (NAI) |
| Project area | Blood & Blood Products |
| Product type | Biologics |
At a glance
- None Citations
- None 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