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FDA Inspection 788644 — Sanofi-Aventis Deutschland GmbH

Sanofi-Aventis Deutschland GmbH — FEI 3003195501

The FDA completed an inspection of Sanofi-Aventis Deutschland GmbH on April 30, 2012 in Frankfurt Am Main. 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
April 30, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Frankfurt Am Main (Germany)

Facility

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Recent compliance actions

FDA data resources