FDA Inspection 676812 — Shionogi Pharma Co., Ltd.

Shionogi Pharma Co., Ltd. — FEI 3002808135

The FDA completed an inspection of Shionogi Pharma Co., Ltd. on Jul 26, 2010 in Isawa-Gun. 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
Jul 26, 2010
Fiscal Year
2010
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Isawa-Gun (Japan)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.