FDA Inspection 1029166 — Pure Valley Water Co
The FDA completed an inspection of Pure Valley Water Co on Oct 13, 2017 in Neosho, MO. 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 13, 2017
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- Neosho, MO (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 1255 | 21 CFR 129.20(a) | Bottling room separation, plant operations |
| 12709 | 21 CFR 129.80(c) | Records - cleaning, sanitizing solutions |
| 1351 | 21 CFR 129.35(a)(3)(i) | Sample frequency - product water |
| 1353 | 21 CFR 129.35(a)(3)(i) | Sample - total coliforms |
| 1761 | 21 CFR 129.80(a) | Records - equipment inspection |
| 1806 | 21 CFR 129.80(b)(1) | Mechanical washers - records |
| 2271 | 21 CFR 129.80(e) | Package identification |
| 2274 | 21 CFR 129.80(g)(1) | Bacteriological test - bottled water |
| 2275 | 21 CFR 129.80(g)(2) | Chemical, physical, radiological tests - bottled water |