FDA Inspection 561065 — Holy Land Factory, LLC.

Holy Land Factory, LLC. — FEI 2000040636

The FDA completed an inspection of Holy Land Factory, LLC. on February 4, 2009 in Minneapolis, MN. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
February 4, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Minneapolis, MN (United States)