# FDA Inspection 954486 - Menicon Co., Ltd. - December 08, 2015

Source: https://www.keypedia.com/records/fda_inspections/menicon-co-ltd/b41fe630-1552-4d63-9408-9e0d438ed8aa
Source feed: FDA_Inspections

> FDA Inspection 954486 for Menicon Co., Ltd. on December 08, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 954486
- Company Name: Menicon Co., Ltd.
- Inspection Date: 2015-12-08
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 954486 - 2015-12-08](https://www.keypedia.com/records/fda_inspections/menicon-co-ltd/36f05114-2c83-45ed-b8d8-269e9744fb9e)

Company: https://www.keypedia.com/companies/menicon-co-ltd/06ba6725-2d31-4f1f-b612-2c297cab7db2

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7