FDA Inspection 777755 — Shionogi Pharma Co. Ltd.

Shionogi Pharma Co. Ltd. — FEI 3008353674

The FDA completed an inspection of Shionogi Pharma Co. Ltd. on Feb 9, 2012 in Tokushima. 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
Feb 9, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tokushima (Japan)

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