FDA Inspection 602314 — Andapharm, LLC

Andapharm, LLC — FEI 3005000348

The FDA completed an inspection of Andapharm, LLC on August 7, 2009 in Fort Lauderdale, FL. 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
August 7, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fort Lauderdale, FL (United States)