FDA Inspection 1327562 — Streamline Manufacturing, LLC
The FDA completed an inspection of Streamline Manufacturing, LLC on Jul 16, 2026 in Lindon, UT. 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). 6 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Jul 16, 2026
- Fiscal Year
- 2026
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Lindon, UT (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15734 | 21 CFR 111.360 | Manufacturing operations - sanitation |
| 15860 | 21 CFR 111.75(a)(2) | Component - confirm identity; specifications met |
| 22843 | 21 CFR 111.70(b) | Specifications - components |
| 22847 | 21 CFR 111.70(e) | Specifications - finished dietary supplement |
| 22862 | 21 CFR 111.105(i) | Quality control - required operations |
| 22884 | 21 CFR 111.205(a) | Master manufacturing record - prepared |