FDA Inspection 1269557 — Melaleuca Inc

Melaleuca Inc — FEI 1000151121

The FDA completed an inspection of Melaleuca Inc on May 14, 2025 in Knoxville, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 14, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Knoxville, TN (United States)

Citations

IDCFRDescription
356721 CFR 211.84(d)(2)Component identification test