FDA Inspection 1058823 — Shiono Finesse, Ltd.
The FDA completed an inspection of Shiono Finesse, Ltd. on June 8, 2018 in Sakai. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions were found but do not meet the threshold for regulatory action). Product area: Drugs.
Inspection Details
- Classification
- Voluntary Action Indicated (VAI) (VAI)
- End Date
- June 8, 2018
- Fiscal Year
- 2018
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Sakai (Japan)