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 Sep 2, 2011 in Notre-Dame-De-Bondeville. 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
Sep 2, 2011
Fiscal Year
2011
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Notre-Dame-De-Bondeville (France)

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