FDA Inspection 1024079 — Omnilife USA, Inc.
The FDA completed an inspection of Omnilife USA, Inc. on Sep 1, 2017 in Commerce, CA. 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). 2 citations were issued during this inspection. Product area: Food/Cosmetics.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 1, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Commerce, CA (United States)
Citations
| ID | CFR | Description |
|---|---|---|
| 15652 | 21 CFR 111.465(b) | Retain reserve samples - 1 year, 2 years |
| 15932 | 21 CFR 111.105(a) | Quality control - processes, specifications, written procedures |