# Okido Ltd. – FDA Inspection, Jun 4, 2010

Source: https://www.keypedia.com/records/fda_inspections/okido-ltd/a8dfdc13-1d7a-44a1-93e9-c9df2793a8c1
Source feed: FDA_Inspections

> FDA inspection 665195 of Okido Ltd., June 04, 2010. Classification: Voluntary Action Indicated (VAI). 2 citations under 21 CFR parts 803 and 820. 2 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 665195
- Company Name: Okido Ltd.
- Inspection Date: 2010-06-04
- 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: 2

## Related Documents

- FDA Inspection 864357 - 2014-01-30
- [FDA Inspection 768169 - 2012-02-17](https://www.keypedia.com/records/fda_inspections/okido-ltd/57ca7be4-30b5-4cc8-a8b3-d1997da822c5)

Company: https://www.keypedia.com/companies/okido-ltd/40aa064a-9b50-4f55-b5ca-c1d82c6147f7

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