# Nidek, Inc. – FDA Inspection, Jul 30, 2013

Source: https://www.keypedia.com/records/fda_inspections/nidek-inc/e5ead85b-5f71-4396-b4df-3abd805cb218
Source feed: FDA_Inspections

> FDA inspection 842321 of Nidek, Inc., July 30, 2013. Classification: Voluntary Action Indicated (VAI). 7 citations under 21 CFR parts 806 and 820. 6 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 842321
- Company Name: Nidek, Inc.
- Inspection Date: 2013-07-30
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 7

## Related Documents

- FDA Inspection 1078121 - 2019-01-24
- [FDA Inspection 1009390 - 2017-03-31](https://www.keypedia.com/records/fda_inspections/nidek-inc/f792cf22-b8f9-4fdd-a305-0bca1a1709d5)
- 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)

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