FDA Inspection 1017506 — Holy Land Factory, LLC.
The FDA completed an inspection of Holy Land Factory, LLC. on July 11, 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). 9 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- July 11, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Minneapolis, MN (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1132 | 21 CFR 110.40(a) | Food-contact - unlawful indirect additives |
| 1406 | 21 CFR 110.10(b)(6) | Effective use of hair restraint |
| 1427 | 21 CFR 110.20(b)(5) | Safety lighting and glass |
| 15391 | 21 CFR 111.10(b)(3) | Hand washing |
| 1553 | 21 CFR 110.35(a) | Buildings/good repair |
| 1554 | 21 CFR 110.35(a) | Cleaning and sanitizing operations |
| 1560 | 21 CFR 110.35(c) | Lack of effective pest exclusion |
| 1562 | 21 CFR 110.35(d) | Failure to clean - general |
| 3661 | 21 CFR 110.37(e)(5) | Signs |