FDA Inspection 1087219 — PureFit Inc

PureFit Inc — FEI 3009801265

The FDA completed an inspection of PureFit Inc on April 11, 2019 in Tustin, CA. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
April 11, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Tustin, CA (United States)