FDA Inspection 570526 — ActiTech, LP

ActiTech, LP — FEI 3007005869

The FDA completed an inspection of ActiTech, LP on March 13, 2009 in Sherman, TX. 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 13, 2009
Fiscal Year
2009
Product Type
Food/Cosmetics
Project Area
Foodborne Biological Hazards
Location
Sherman, TX (United States)