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FDA Inspection 1174998 — Aspen Notre Dame de Bondeville

Aspen Notre Dame de Bondeville — FEI 3002808079

The FDA completed an inspection of Aspen Notre Dame de Bondeville on April 16, 2021 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
April 16, 2021
Fiscal Year
2021
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Notre-Dame-De-Bondeville (France)

Additional Details

Mutual Recognition Agreement (MRA)

Facility

Other inspections at this facility

  • 1309944 (VAI Fri Nov 07 2025 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 1058932 (NAI Thu May 31 2018 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 988923 (NAI Tue Aug 30 2016 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 850923 (NAI Tue Sep 17 2013 00:00:00 GMT+0000 (Coordinated Universal Time))
  • 749604 (VAI Fri Sep 02 2011 00:00:00 GMT+0000 (Coordinated Universal Time))

FDA data resources