FDA Inspection 829250 — Umeken USA, Inc.

Umeken USA, Inc. — FEI 3004328994

The FDA completed an inspection of Umeken USA, Inc. on Apr 24, 2013 in Cerritos, CA. 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
Apr 24, 2013
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Cerritos, CA (United States)

Citations

IDCFRDescription
1564121 CFR 111.453Written procedures - holding
1579721 CFR 111.553Written procedures - product complaint
1604221 CFR 111.503Written procedures - returned dietary supplement