FDA inspection
Anacapa Technologies Inc: FDA inspection ending Mar 19, 2003
FDA inspection 264485 · Voluntary Action Indicated (VAI) · San Dimas, CA
Key facts
| Inspection ID | 264485 |
|---|---|
| Firm | Anacapa Technologies Inc |
| FEI number | 3003693789 |
| Address | 301 E Arrow Hwy |
| City | San Dimas |
| State | CA |
| ZIP | 91773-3364 |
| Fiscal year | 2003 |
| Inspection end date | Mar 19, 2003 |
| 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
- Yes 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