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FDA Inspection 1091022 — Melaleuca Inc

Melaleuca Inc — FEI 1000151121

The FDA completed an inspection of Melaleuca Inc on May 10, 2019 in Knoxville, TN. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 10, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Knoxville, TN (United States)

Facility

Other inspections at this facility

  • 1269557 (VAI Wed May 14 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 952520 (NAI Fri Dec 18 2015 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 892909 (NAI Thu Aug 28 2014 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 773409 (NAI Tue Mar 06 2012 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 615783 (NAI Thu Sep 24 2009 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources