FDA Inspection 770009 — Sumitomo Pharma Co., Ltd.

Sumitomo Pharma Co., Ltd. — FEI 3003028650

The FDA completed an inspection of Sumitomo Pharma Co., Ltd. on Feb 23, 2012 in Suzuka. 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: Veterinary.

Inspection Details

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

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