# Nidek Medical Products Inc - Inspection Records

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

> Inspection records and compliance data for Nidek Medical Products Inc in Birmingham, Alabama. Access full analysis and detailed observations.

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## Details

- Name: Nidek Medical Products Inc
- FEI Number: 1039215
- City: Birmingham
- State: Alabama
- Country Name: United States
- Address Line 1: 3949 Valley East Industrial Dr
- Zip Code: 35217

## Related Documents

- [FDA Inspection 985390 - Nidek Medical Products Inc - 2016-08-16](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/afdfab4f-b3b5-42c0-8c6f-79ff941812eb) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2016
- [FDA Inspection 985390 - Nidek Medical Products Inc - 2016-08-16](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/d53d8b93-c9ba-49af-a9f3-5ae42c8f436d) — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2016
- [FDA Inspection 855858 - Nidek Medical Products Inc - 2013-11-20](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/25eee11d-4806-4f72-ad61-f4decded9365) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2013
- [FDA Inspection 855858 - Nidek Medical Products Inc - 2013-11-20](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/4d4bd29d-82c5-4779-a5d1-08a53ae093da) — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2013
- [FDA Inspection 775100 - Nidek Medical Products Inc - 2012-04-10](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/787d5e76-4119-46a1-8dbb-21e7be363299) — classification: Official Action Indicated (OAI), source: FDA, date: April 10, 2012
- [FDA Inspection 775100 - Nidek Medical Products Inc - 2012-04-10](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/a707df96-3472-4c78-a0e6-26e93b270d0c) — classification: Official Action Indicated (OAI), source: FDA, date: April 10, 2012
- [FDA Inspection 650979 - Nidek Medical Products Inc - 2010-02-24](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/d6ba1a14-3b04-49ab-bd8a-320d18682af1) — classification: Voluntary Action Indicated (VAI), source: FDA, date: February 24, 2010

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