FDA Inspection 1250788 — Abraham Borntrager
The FDA completed an inspection of Abraham Borntrager on Oct 2, 2024 in Augusta, WI. 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). 9 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Oct 2, 2024
- Fiscal Year
- 2025
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Augusta, WI (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 16120 | 21 CFR 118.4 | Written SE plan lacks required elements |
| 16122 | 21 CFR 118.4(a)(2)(i) | Pullet environment testing |
| 16131 | 21 CFR 118.4(b) | Transfer or introduction of SE |
| 16149 | 21 CFR 118.4(e) | Egg transport temperature/time |
| 16183 | 21 CFR 118.9 | Supervisor(s) training/job experience |
| 16197 | 21 CFR 118.10(a)(3)(vi) | SE testing results documentation |
| 16202 | 21 CFR 118.10(e) | Official review and copying of records |
| 16203 | 21 CFR 118.10(b)(1) | Name and location |
| 16209 | 21 CFR 118.11(a) | Registration within 30 days |