FDA Inspection 853865 — Sumitomo Pharma Co., Ltd.
The FDA completed an inspection of Sumitomo Pharma Co., Ltd. on Nov 1, 2013 in Suzuka. 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
- Nov 1, 2013
- Fiscal Year
- 2014
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Suzuka (Japan)