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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 August 30, 2016 in Notre-Dame-De-Bondeville. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
August 30, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Notre-Dame-De-Bondeville (France)

Facility

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