FDA Inspection 1277062 — Moringa Pura Vida S.A.

Moringa Pura Vida S.A. — FEI 3016058753

The FDA completed an inspection of Moringa Pura Vida S.A. on Jul 31, 2025 in Upala. 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). 5 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 31, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Upala (Costa Rica)

Citations

IDCFRDescription
1583821 CFR 111.70(d)Specifications - labels, packaging
2284321 CFR 111.70(b)Specifications - components
2284721 CFR 111.70(e)Specifications - finished dietary supplement
2285921 CFR 111.103Written procedures - establish; quality control operations
2288421 CFR 111.205(a)Master manufacturing record - prepared

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.