# FDA Inspection 665195 - Okido Ltd. - June 04, 2010

Source: https://www.keypedia.com/records/fda_inspections/okido-ltd/3e924d28-0ab9-43dd-ac03-63e4937ad2bb
Source feed: FDA_Inspections

> FDA Inspection 665195 for Okido Ltd. on June 04, 2010. Classification: Voluntary Action Indicated (VAI).

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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)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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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