FDA Inspection 1087840 — Taisho Pharmaceutical Co., Ltd.
The FDA completed an inspection of Taisho Pharmaceutical Co., Ltd. on Mar 29, 2019 in Saitama. 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
- Mar 29, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Saitama (Japan)