FDA Inspection 933845 — Sanofi Aventis Singapore Pte. Ltd.

Sanofi Aventis Singapore Pte. Ltd. — FEI 3003091951

The FDA completed an inspection of Sanofi Aventis Singapore Pte. Ltd. on May 22, 2015 in Singapore. 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
May 22, 2015
Fiscal Year
2015
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Singapore (Singapore)

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