FDA Inspection 962514 — Herbalife Manufacturing, LLC

Herbalife Manufacturing, LLC — FEI 3007696780

The FDA completed an inspection of Herbalife Manufacturing, LLC on Mar 9, 2016 in Lake Forest, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Mar 9, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Lake Forest, CA (United States)

Citations

IDCFRDescription
1575021 CFR 111.210(d)Master manufacturing record - ingredients list
1575121 CFR 111.210(d)Master manufacturing record - Supplemental Facts