FDA Inspection 1325658 — Carefast Products Inc

Carefast Products Inc — FEI 3014804875

The FDA completed an inspection of Carefast Products Inc on Jul 8, 2026 in Las Vegas, NV. 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). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jul 8, 2026
Fiscal Year
2026
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Las Vegas, NV (United States)

Citations

IDCFRDescription
2281121 CFR 111.453Written procedures - establish; holding and distribution
2281321 CFR 111.553Written procedures - establish; product complaint
2290821 CFR 111.503Written procedures - establish; returned dietary supplements

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