FDA Inspection 950162 — Shionogi Pharma Co. Ltd.

Shionogi Pharma Co. Ltd. — FEI 3008353674

The FDA completed an inspection of Shionogi Pharma Co. Ltd. on Dec 4, 2015 in Tokushima. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Dec 4, 2015
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Tokushima (Japan)

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