FDA Inspection 1073580 — Omnilife Manufactura S.A. de C.V.
The FDA completed an inspection of Omnilife Manufactura S.A. de C.V. on December 6, 2018 in Tlaquepaque. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 1 citation was issued during this inspection. Product area: Food/Cosmetics.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- December 6, 2018
- Fiscal Year
- 2019
- Product Type
- Food/Cosmetics
- Project Area
- Food Composition, Standards, Labeling and Econ
- Location
- Tlaquepaque (Mexico)
Citations
| ID | CFR | Description |
|---|---|---|
| 15821 | 21 CFR 111.60(a) | Production, in- process control system - design, quality |