# FDA Inspection 985390 - Nidek Medical Products Inc - August 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/d53d8b93-c9ba-49af-a9f3-5ae42c8f436d
Source feed: FDA_Inspections

> FDA Inspection 985390 for Nidek Medical Products Inc on August 16, 2016. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 985390
- Company Name: Nidek Medical Products Inc
- Inspection Date: 2016-08-16
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 985390 - 2016-08-16](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/afdfab4f-b3b5-42c0-8c6f-79ff941812eb)
- [FDA Inspection 855858 - 2013-11-20](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/4d4bd29d-82c5-4779-a5d1-08a53ae093da)
- [FDA Inspection 855858 - 2013-11-20](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/25eee11d-4806-4f72-ad61-f4decded9365)
- [FDA Inspection 775100 - 2012-04-10](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/a707df96-3472-4c78-a0e6-26e93b270d0c)
- [FDA Inspection 775100 - 2012-04-10](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/787d5e76-4119-46a1-8dbb-21e7be363299)

Company: https://www.keypedia.com/companies/nidek-medical-products-inc/8fe620e0-7ed2-450b-87e1-8aebea515bd8

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