FDA Inspection 1127299 — Bioiberica, SAU

Bioiberica, SAU — FEI 1000418405

The FDA completed an inspection of Bioiberica, SAU on December 17, 2019 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
December 17, 2019
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Palafolls (Spain)

Additional Details

Mutual Recognition Agreement (MRA)