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FDA Inspection 770009 — Sumitomo Pharma Co., Ltd.

Sumitomo Pharma Co., Ltd. — FEI 3003028650

The FDA completed an inspection of Sumitomo Pharma Co., Ltd. on February 23, 2012 in Suzuka. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Veterinary.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
February 23, 2012
Fiscal Year
2012
Product Type
Veterinary
Project Area
Monitoring of Marketed Animal Drugs, Feed, and Devices
Location
Suzuka (Japan)

Facility

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