FDA Inspection 954486 — Menicon Co., Ltd.
The FDA completed an inspection of Menicon Co., Ltd. on Dec 8, 2015 in Nagoya. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Dec 8, 2015
- Fiscal Year
- 2016
- Product Type
- Devices
- Project Area
- Compliance: Devices
- Location
- Nagoya (Japan)