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FDA Inspection 749604 — Aspen Notre Dame de Bondeville

Aspen Notre Dame de Bondeville — FEI 3002808079

The FDA completed an inspection of Aspen Notre Dame de Bondeville on September 2, 2011 in Notre-Dame-De-Bondeville. 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
September 2, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Notre-Dame-De-Bondeville (France)

Facility

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FDA data resources