# FDA Inspection 1078121 - Nidek, Inc. - January 24, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/0b8d6b29-9ef5-49f4-87f6-0a7b8a6fe0a6
Source feed: FDA_Inspections

> FDA Inspection 1078121 for Nidek, Inc. on January 24, 2019. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1078121
- Company Name: Nidek, Inc.
- Inspection Date: 2019-01-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1078121 - 2019-01-24](https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/9aefb102-868a-4f7a-84d1-cd6cf6a23049)
- [FDA Inspection 1078121 - 2019-01-24](https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/41c1d26e-6c9a-440e-82a2-43b983a58da0)
- [FDA Inspection 1009390 - 2017-03-31](https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/f792cf22-b8f9-4fdd-a305-0bca1a1709d5)
- [FDA Inspection 1009390 - 2017-03-31](https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/d16d523b-c000-438c-915b-8517335d582e)
- [FDA Inspection 980717 - 2016-08-10](https://www.globalkeysolutions.net/records/fda_inspections/nidek-inc/f95e84c0-d7bc-429b-828f-7e46a0c3a362)

Company: https://www.globalkeysolutions.net/companies/nidek-inc/f2d405a1-3f0a-4f61-bf90-c798bf18385b

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