FDA Inspection 1064584 — Sumitomo Pharma Co., Ltd.

Sumitomo Pharma Co., Ltd. — FEI 3003028650

The FDA completed an inspection of Sumitomo Pharma Co., Ltd. on July 27, 2018 in Suzuka. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Drugs.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 27, 2018
Fiscal Year
2018
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Suzuka (Japan)