FDA Inspection 1264836 — Fulex LLC

Fulex LLC — FEI 3019867798

The FDA completed an inspection of Fulex LLC on Mar 25, 2025 in Chattanooga, TN. 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
Mar 25, 2025
Fiscal Year
2025
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Chattanooga, TN (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.