FDA Inspection 1116659 — Cenexi

Cenexi — FEI 3007250542

The FDA completed an inspection of Cenexi on June 19, 2018 in Fontenay-Sous-Bois. 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
June 19, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fontenay-Sous-Bois (France)

Additional Details

Mutual Recognition Agreement (MRA)