FDA Inspection 974988 — Libido Edge Labs, LLC

Libido Edge Labs, LLC — FEI 3008152246

The FDA completed an inspection of Libido Edge Labs, LLC on June 2, 2016 in Newark, OH. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Food/Cosmetics.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 2, 2016
Fiscal Year
2016
Product Type
Food/Cosmetics
Project Area
Colors and Cosmetics Technology
Location
Newark, OH (United States)