FDA Inspection 1105208 — ActiTech, LP

ActiTech, LP — FEI 3007005869

The FDA completed an inspection of ActiTech, LP on September 25, 2019 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
September 25, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Sherman, TX (United States)