FDA Inspection 1323186 — UCB Pharma S.A.

UCB Pharma S.A. — FEI 3003909356

The FDA completed an inspection of UCB Pharma S.A. on Jun 4, 2026 in Braine-L'Alleud. 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). 2 citations were issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Jun 4, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Braine-L'Alleud (Belgium)

Citations

IDCFRDescription
23087ISO 13485:2016 Clause 7.1Product realization risk management processes not documented
23258ISO 13485:2016 Clause 8.5.2Corrective action procedures not documented

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