FDA Inspection 988923 — Aspen Notre Dame De Bondeville

Aspen Notre Dame De Bondeville — FEI 3002808079

The FDA completed an inspection of Aspen Notre Dame De Bondeville on Aug 30, 2016 in Notre-Dame-De-Bondeville. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection details

Classification
No Action Indicated (NAI)
End Date
Aug 30, 2016
Fiscal Year
2016
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.