FDA inspection
Allermed Laboratories, Inc.: FDA inspection ending Nov 12, 2018
FDA inspection 1071500 · Voluntary Action Indicated (VAI) · San Diego, CA
Key facts
| Inspection ID | 1071500 |
|---|---|
| Firm | Allermed Laboratories, Inc. |
| FEI number | 1000098920 |
| Address | 7203 Convoy Ct |
| City | San Diego |
| State | CA |
| ZIP | 92111 |
| Country | United States |
| Fiscal year | 2019 |
| Inspection end date | Nov 12, 2018 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Vaccines and Allergenic Products |
| Product type | Biologics |
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
- 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