FDA Inspection 976108 — Cenexi

Cenexi — FEI 3007250542

The FDA completed an inspection of Cenexi on Apr 6, 2016 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
Apr 6, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Fontenay-Sous-Bois (France)

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