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