FDA inspection
Herbalife Manufacturing, LLC: FDA inspection ending Sep 11, 2013
FDA inspection 849137 · Voluntary Action Indicated (VAI) · Lake Forest, CA
Key facts
| Inspection ID | 849137 |
|---|---|
| Firm | Herbalife Manufacturing, LLC |
| FEI number | 3007696780 |
| Address | 20481 Crescent Bay Dr |
| City | Lake Forest |
| State | CA |
| ZIP | 92630 |
| Country | United States |
| Fiscal year | 2013 |
| Inspection end date | Sep 11, 2013 |
| Classification | Voluntary Action Indicated (VAI) |
| Project area | Foodborne Biological Hazards |
| Product type | Food/Cosmetics |
At a glance
- 10–99 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