FDA inspection
Anacapa Technologies Inc: FDA inspection ending Jul 23, 2007
FDA inspection 480261 · Voluntary Action Indicated (VAI) · San Dimas, CA
Key facts
| Inspection ID | 480261 |
|---|---|
| Firm | Anacapa Technologies Inc |
| FEI number | 3003693789 |
| Address | 301 E Arrow Hwy |
| City | San Dimas |
| State | CA |
| ZIP | 91773-3364 |
| Fiscal year | 2007 |
| Inspection end date | Jul 23, 2007 |
| 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