FDA Inspection 638332 — Kellanova Manufacturing

Kellanova Manufacturing — FEI 1039607

The FDA completed an inspection of Kellanova Manufacturing on Dec 11, 2009 in Rome, GA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Dec 11, 2009
Fiscal Year
2010
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Rome, GA (United States)

Citations

IDCFRDescription
128921 CFR 110.20(a)(3)Drainage
130621 CFR 110.20(b)(7)Screening
142221 CFR 110.20(b)(4)Floors, walls and ceilings