FDA Inspection 1105208 — ActiTech, LP

ActiTech, LP — FEI 3007005869

The FDA completed an inspection of ActiTech, LP on Sep 25, 2019 in Sherman, TX. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Food/Cosmetics.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Sep 25, 2019
Fiscal Year
2019
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Sherman, TX (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.