# NIDEK Co., Ltd. – FDA Inspection, Jul 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 of NIDEK Co., Ltd., July 31, 2014. 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: 890755
- Company Name: NIDEK Co., Ltd.
- Inspection Date: 2014-07-31
- 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: 6

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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