FDA Inspection 809078 — Omnilife Manufactura S.A. de C.V.

Omnilife Manufactura S.A. de C.V. — FEI 3004266321

The FDA completed an inspection of Omnilife Manufactura S.A. de C.V. on November 27, 2012 in Tlaquepaque. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 2 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
November 27, 2012
Fiscal Year
2013
Product Type
Food/Cosmetics
Project Area
Food Composition, Standards, Labeling and Econ
Location
Tlaquepaque (Mexico)

Citations

IDCFRDescription
1573921 CFR 111.210(h)(3)(ii)(B)Components; add, verify
1588521 CFR 111.77(a)Specifications not met - reject, quality control