FDA Inspection 1011322 — Holy Land Brand Inc.

Holy Land Brand Inc. — FEI 3013439486

The FDA completed an inspection of Holy Land Brand Inc. on Apr 19, 2017 in Minneapolis, MN. 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 19, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Minneapolis, MN (United States)

Citations

IDCFRDescription
142721 CFR 110.20(b)(5)Safety lighting and glass
156021 CFR 110.35(c)Lack of effective pest exclusion
365221 CFR 110.37(e)(1)Suitable locations

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.