FDA Inspection 1247808 — UCB Pharma S.A.

UCB Pharma S.A. — FEI 3003909356

The FDA completed an inspection of UCB Pharma S.A. on Feb 1, 2024 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). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 1, 2024
Fiscal Year
2024
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Braine-L'Alleud (Belgium)

Additional Details

Mutual Recognition Agreement (MRA)

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