FDA Inspection 1222240 — Biofer Spa

Biofer Spa — FEI 3005593220

The FDA completed an inspection of Biofer Spa on September 30, 2022 in Medolla. 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
September 30, 2022
Fiscal Year
2022
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Medolla (Italy)

Additional Details

Mutual Recognition Agreement (MRA)