FDA Inspection 1117682 — Daito Pharmaceutical Co., Ltd.

Daito Pharmaceutical Co., Ltd. — FEI 3002806779

The FDA completed an inspection of Daito Pharmaceutical Co., Ltd. on Jan 31, 2020 in Toyama. The inspection was classified OAI (Official Action Indicated — objectionable conditions were found and regulatory action is recommended). Product area: Drugs.

Inspection Details

Classification
Official Action Indicated (OAI)
End Date
Jan 31, 2020
Fiscal Year
2020
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Toyama (Japan)