FDA Inspection 1276304 — FIS - Fabbrica Italiana Sintetici SpA

FIS - Fabbrica Italiana Sintetici SpA — FEI 3002808541

The FDA completed an inspection of FIS - Fabbrica Italiana Sintetici SpA on October 28, 2022 in Lonigo. 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
October 28, 2022
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Lonigo (Italy)

Additional Details

Mutual Recognition Agreement (MRA)