FDA Inspection 942411 — OMNILIFE USA INC
The FDA completed an inspection of OMNILIFE USA INC on Sep 11, 2015 in Cicero, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 11, 2015
- Fiscal Year
- 2015
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Cicero, IL (United States)