FDA Inspection 946034 — Mizuho Corporation Gosen Factory
The FDA completed an inspection of Mizuho Corporation Gosen Factory on Sep 3, 2015 in Gosen. 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: Devices.
Inspection details
- Classification
- Voluntary Action Indicated (VAI)
- End Date
- Sep 3, 2015
- Fiscal Year
- 2015
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Gosen (Japan)