FDA Inspection 1064584 — Sumitomo Pharma Co., Ltd.

Sumitomo Pharma Co., Ltd. — FEI 3003028650

The FDA completed an inspection of Sumitomo Pharma Co., Ltd. on Jul 27, 2018 in Suzuka. 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
Jul 27, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Suzuka (Japan)

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