# FDA Inspection 890755 - NIDEK Co., Ltd. - July 31, 2014

Source: https://www.keypedia.com/records/fda_inspections/nidek-co-ltd/b6b760a2-6afe-4e60-9094-42ffde903029
Source feed: FDA_Inspections

> FDA Inspection 890755 for NIDEK Co., Ltd. on July 31, 2014. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 890755
- Company Name: NIDEK Co., Ltd.
- Inspection Date: 2014-07-31
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 890755 - 2014-07-31](https://www.keypedia.com/records/fda_inspections/nidek-co-ltd/b2f6730d-c3ec-4861-981d-860e6341a18d)
- [FDA Inspection 653387 - 2010-02-18](https://www.keypedia.com/records/fda_inspections/nidek-co-ltd/fd71e503-6110-469b-ae9c-08cdcccb6fc7)

Company: https://www.keypedia.com/companies/nidek-co-ltd/d2c1c127-d4a8-47b8-817c-27d56c77492e

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