FDA Inspection 1082203 — Palouse Pulse LLC

Palouse Pulse LLC — FEI 3020739

The FDA completed an inspection of Palouse Pulse LLC on Feb 19, 2019 in Farmington, WA. 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
Feb 19, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Farmington, WA (United States)