FDA Inspection 569116 — Melaleuca Inc

Melaleuca Inc — FEI 3021937

The FDA completed an inspection of Melaleuca Inc on Feb 6, 2009 in Idaho Falls, ID. 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). 4 citations were issued during this inspection. Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 6, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Idaho Falls, ID (United States)

Citations

IDCFRDescription
110521 CFR 211.22(d)Procedures not in writing, fully followed
355921 CFR 211.56(a)Sanitation--buildings not clean, free of infestation
361621 CFR 211.165(d)Acceptance criteria for sampling & testing
437221 CFR 211.188(b)(8)Labeling control records including specimens or copies

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