FDA Warning Letter — Libido Edge Labs, LLC

Case 94106 — FEI 3008152246

The FDA took a Warning Letter action against Libido Edge Labs, LLC on June 10, 2010 (Newark, OH). The action was issued by CDER and concerns drugs products. This facility has 3 recent FDA inspections on record.

Action Details

Facility
Libido Edge Labs, LLC
Date
June 10, 2010
Fiscal Year
2010
Product Type
Drugs
Center
CDER
Location
Newark, OH (United States)