FDA Inspection 1100505 — Toyobo Co. Ltd.
The FDA completed an inspection of Toyobo Co. Ltd. on July 30, 2019 in Otsu. 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
- July 30, 2019
- Fiscal Year
- 2019
- Product Type
- Drugs
- Project Area
- Drug Quality Assurance
- Location
- Otsu (Japan)