FDA Inspection 1014171 — Sid Kurlander and Son, Inc.

Sid Kurlander and Son, Inc. — FEI 3004145490

The FDA completed an inspection of Sid Kurlander and Son, Inc. on May 25, 2017 in Santa Rosa, CA. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 25, 2017
Fiscal Year
2017
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Santa Rosa, CA (United States)