FDA inspection
Ajinomoto Althea, Inc.: FDA inspection ending Mar 22, 2019
FDA inspection 1088015 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 1088015 |
|---|---|
| Firm | Ajinomoto Althea, Inc. |
| FEI number | 3004575449 |
| Address | 11040 Roselle St |
| City | San Diego |
| State | CA |
| ZIP | 92121-1205 |
| Fiscal year | 2019 |
| Inspection end date | Mar 22, 2019 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | New Drug Evaluation |
| Product type | Drugs |
At a glance
- None Citations
- 1–9 Posted citations
- No Warning letter followed
- Yes Form FDA 483 issued
- Yes Establishment inspection report (EIR) exists
- 10–99 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