FDA Inspection 714985 — Apex360, LLC

Apex360, LLC — FEI 3006358789

The FDA completed an inspection of Apex360, LLC on March 11, 2011 in Burlington, KY. 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
March 11, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Burlington, KY (United States)