# FDA Inspection 954844 - Menicon Nect Co., Ltd., Gujo Plant - December 11, 2015

Source: https://www.keypedia.com/records/fda_inspections/menicon-nect-co-ltd-gujo-plant/22aee23d-ee5a-4179-9168-36ea7157b61d
Source feed: FDA_Inspections

> FDA Inspection 954844 for Menicon Nect Co., Ltd., Gujo Plant on December 11, 2015. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 954844
- Company Name: Menicon Nect Co., Ltd., Gujo Plant
- Inspection Date: 2015-12-11
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

Company: https://www.keypedia.com/companies/menicon-nect-co-ltd-gujo-plant/053c5495-6989-4e14-915e-d342c6c20a7b

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