FDA Inspection 1294708 — Marina Elena Cazzaniga, MD

Marina Elena Cazzaniga, MD — FEI 3039147426

The FDA completed an inspection of Marina Elena Cazzaniga, MD on Nov 21, 2025 in Monza. 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 21, 2025
Fiscal Year
2026
Product Type
Drugs
Project Area
Bioresearch Monitoring
Location
Monza (Italy)

Additional Details

Clinical Investigator (CI)

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