FDA Inspection 734276 — PureTek Corporation

PureTek Corporation — FEI 1000125324

The FDA completed an inspection of PureTek Corporation on March 16, 2011 in San Fernando, 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
March 16, 2011
Fiscal Year
2011
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
San Fernando, CA (United States)