FDA Inspection 1080814 — Daiichi Sankyo Co., Ltd.

Daiichi Sankyo Co., Ltd. — FEI 3002808054

The FDA completed an inspection of Daiichi Sankyo Co., Ltd. on Jan 18, 2019 in Iwaki. 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
Jan 18, 2019
Fiscal Year
2019
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Iwaki (Japan)

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