# Nidek Medical Products Inc – FDA Inspection, Feb 24, 2010

Source: https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/d6ba1a14-3b04-49ab-bd8a-320d18682af1
Source feed: FDA_Inspections

> FDA inspection 650979 of Nidek Medical Products Inc, February 24, 2010. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 4 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 650979
- Company Name: Nidek Medical Products Inc
- Inspection Date: 2010-02-24
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 6

## Related Documents

- [FDA Inspection 1042510 - 2017-10-19](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/bd9fbee0-1b28-4c1d-aa90-c2a838fc44b8)
- FDA Inspection 985390 - 2016-08-16
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- [FDA Inspection 775100 - 2012-04-10](https://www.keypedia.com/records/fda_inspections/nidek-medical-products-inc/a707df96-3472-4c78-a0e6-26e93b270d0c)

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