FDA Inspection 676812 — Shionogi Pharma Co., Ltd.

Shionogi Pharma Co., Ltd. — FEI 3002808135

The FDA completed an inspection of Shionogi Pharma Co., Ltd. on July 26, 2010 in Isawa-Gun. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI) (VAI)
End Date
July 26, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Isawa-Gun (Japan)