FDA Inspection 663582 — ActiTech, LP

ActiTech, LP — FEI 3007005869

The FDA completed an inspection of ActiTech, LP on May 24, 2010 in Sherman, TX. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). 3 citations were issued during this inspection. Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
May 24, 2010
Fiscal Year
2010
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Sherman, TX (United States)

Citations

IDCFRDescription
136121 CFR 211.100(a)Absence of Written Procedures
194221 CFR 211.180(e)Records reviewed annually
360221 CFR 211.160(a)Deviations from laboratory control requirements