FDA Inspection 1342184 — Fresenius Kabi iPSUM S.R.L..

Fresenius Kabi iPSUM S.R.L.. — FEI 3004938331

The FDA completed an inspection of Fresenius Kabi iPSUM S.R.L.. on Jul 10, 2025 in Vicchio. 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
Jul 10, 2025
Fiscal Year
2025
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Vicchio (Italy)

Additional Details

Mutual Recognition Agreement (MRA)

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