FDA Inspection 633571 — Corden Pharma Chenove

Corden Pharma Chenove — FEI 3002808295

The FDA completed an inspection of Corden Pharma Chenove on November 20, 2009 in Chenove. 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
November 20, 2009
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Chenove (France)