FDA Inspection 1321352 — Cebiphar

Cebiphar — FEI 3004104539

The FDA completed an inspection of Cebiphar on January 20, 2023 in Fondettes. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
January 20, 2023
Fiscal Year
2023
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fondettes (France)

Additional Details

Mutual Recognition Agreement (MRA)