FDA Inspection 1026870 — OMNILIFE USA, Inc.
The FDA completed an inspection of OMNILIFE USA, Inc. on Sep 8, 2017 in San Jose, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.
Inspection details
- Classification
- No Action Indicated (NAI)
- End Date
- Sep 8, 2017
- Fiscal Year
- 2017
- Product Type
- Food/Cosmetics
- Project Area
- Foodborne Biological Hazards
- Location
- San Jose, CA (United States)