FDA Inspection 1119539 — Leo Pharma Manufacturing Italy SRL

Leo Pharma Manufacturing Italy SRL — FEI 3002808260

The FDA completed an inspection of Leo Pharma Manufacturing Italy SRL on July 25, 2019 in Segrate. 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
July 25, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Segrate (Italy)

Additional Details

Mutual Recognition Agreement (MRA)