# Nidek Medical Products Inc, Birmingham, AL – FDA Inspections

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. 5 FDA inspections on record (1 OAI), 1 Form 483, last inspected October 19, 2017.

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## Details

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

## Related Documents

- [FDA Inspection 1042510 - Nidek Medical Products Inc - 2017-10-19](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/bd9fbee0-1b28-4c1d-aa90-c2a838fc44b8) — source: FDA, date: October 19, 2017
- FDA Inspection 985390 - Nidek Medical Products Inc - 2016-08-16 — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2016
- FDA Inspection 985390 - Nidek Medical Products Inc - 2016-08-16 — classification: No Action Indicated (NAI), source: FDA, date: August 16, 2016
- FDA Inspection 855858 - Nidek Medical Products Inc - 2013-11-20 — classification: No Action Indicated (NAI), source: FDA, date: November 20, 2013
- FDA Inspection 855858 - Nidek Medical Products Inc - 2013-11-20 — 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/a707df96-3472-4c78-a0e6-26e93b270d0c) — classification: Official Action Indicated (OAI), source: FDA, date: April 10, 2012
- FDA Inspection 775100 - Nidek Medical Products Inc - 2012-04-10 — 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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