FDA Inspection 1268874 — Leo Pharma Manufacturing Italy SRL

Leo Pharma Manufacturing Italy SRL — FEI 3002808260

The FDA completed an inspection of Leo Pharma Manufacturing Italy SRL on Nov 30, 2023 in Segrate. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection details

Classification
Voluntary Action Indicated (VAI)
End Date
Nov 30, 2023
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Segrate (Italy)

Additional details

Mutual Recognition Agreement (MRA)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.