FDA Inspection 728488 — Libido Edge Labs, LLC

Libido Edge Labs, LLC — FEI 3008152246

The FDA completed an inspection of Libido Edge Labs, LLC on June 6, 2011 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: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
June 6, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Unapproved and Misbranded Drugs
Location
Newark, OH (United States)