FDA Inspection 825670 — Bioiberica, SAU

Bioiberica, SAU — FEI 1000418405

The FDA completed an inspection of Bioiberica, SAU on November 22, 2012 in Palafolls. 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
November 22, 2012
Fiscal Year
2013
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Palafolls (Spain)