FDA Inspection 1011322 — Holy Land Brand Inc.
The FDA completed an inspection of Holy Land Brand Inc. on April 19, 2017 in Minneapolis, MN. 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) (VAI)
- End Date
- April 19, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Minneapolis, MN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1427 | 21 CFR 110.20(b)(5) | Safety lighting and glass |
| 1560 | 21 CFR 110.35(c) | Lack of effective pest exclusion |
| 3652 | 21 CFR 110.37(e)(1) | Suitable locations |