FDA Inspection 953176 — Demeter LP

Demeter LP — FEI 3004387565

The FDA completed an inspection of Demeter LP on Oct 14, 2015 in Woodstock, IL. 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
Oct 14, 2015
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Woodstock, IL (United States)