FDA Inspection 987969 — Teikoku Seiyaku Co., Ltd.

Teikoku Seiyaku Co., Ltd. — FEI 3002808398

The FDA completed an inspection of Teikoku Seiyaku Co., Ltd. on Sep 9, 2016 in Higashikagawa. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). Product area: Drugs.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 9, 2016
Fiscal Year
2016
Product Type
Drugs
Project Area
Drug Quality Assurance
Location
Higashikagawa (Japan)