# Nidek, Inc. – FDA Inspection, Mar 31, 2017

Source: https://www.keypedia.com/records/fda_inspections/nidek-inc/f792cf22-b8f9-4fdd-a305-0bca1a1709d5
Source feed: FDA_Inspections

> FDA inspection 1009390 of Nidek, Inc., March 31, 2017. Classification: No Action Indicated (NAI). 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1009390
- Company Name: Nidek, Inc.
- Inspection Date: 2017-03-31
- Classification: No Action Indicated (NAI)
- Classification Code: NAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 0

## Related Documents

- FDA Inspection 1078121 - 2019-01-24
- FDA Inspection 980717 - 2016-08-10
- FDA Inspection 930830 - 2015-06-10
- [FDA Inspection 871244 - 2014-04-14](https://www.keypedia.com/records/fda_inspections/nidek-inc/df775622-b46b-4152-b089-a23899e002d8)
- [FDA Inspection 842321 - 2013-07-30](https://www.keypedia.com/records/fda_inspections/nidek-inc/e5ead85b-5f71-4396-b4df-3abd805cb218)

## Related Officers

- [Investigator](https://www.keypedia.com/people/jude-c-dike/ea760122-1121-420a-9875-c49de6f3bb0e)

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

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