FDA Inspection 954889 — Menicon Co., Ltd. Central Research Laboratory
The FDA completed an inspection of Menicon Co., Ltd. Central Research Laboratory on Dec 10, 2015 in Kasugai. 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
- Dec 10, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Kasugai (Japan)