FDA Inspection 1116659 — Cenexi

Cenexi — FEI 3007250542

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

Additional details

Mutual Recognition Agreement (MRA)

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