FDA Inspection 602314 — Andapharm, LLC

Andapharm, LLC — FEI 3005000348

The FDA completed an inspection of Andapharm, LLC on Aug 7, 2009 in Fort Lauderdale, FL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Aug 7, 2009
Fiscal Year
2009
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fort Lauderdale, FL (United States)

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