FDA Inspection 1087085 — Herbalife Manufacturing, LLC
The FDA completed an inspection of Herbalife Manufacturing, LLC on Feb 19, 2019 in Lake Forest, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Feb 19, 2019
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Lake Forest, CA (United States)