FDA Inspection 777783 — Shionogi Pharma Co., Ltd.

Shionogi Pharma Co., Ltd. — FEI 3006396183

The FDA completed an inspection of Shionogi Pharma Co., Ltd. on Feb 15, 2012 in Amagasaki. 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 15, 2012
Fiscal Year
2012
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Amagasaki (Japan)