FDA Inspection 1029438 — VitaPurity Corporation
The FDA completed an inspection of VitaPurity Corporation on October 13, 2017 in Central Point, OR. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 5 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- October 13, 2017
- Fiscal Year
- 2018
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Central Point, OR (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15659 | 21 CFR 111.475(b)(1) | Written procedures - holding; distributing |
| 15797 | 21 CFR 111.553 | Written procedures - product complaint |
| 15920 | 21 CFR 111.95(b)(1) | Records - established specifications |
| 15995 | 21 CFR 111.127(d) | Quality control operations - packaged, labeled; specifications |
| 16057 | 21 CFR 111.535(b)(1) | Records - returned dietary supplement: written procedures |