# FDA Inspection 772787 - Omron Healthcare, Inc. - March 22, 2012

Source: https://www.keypedia.com/records/fda_inspections/omron-healthcare-inc/9a9013fa-005f-4bfd-9b60-480ad2fb2100
Source feed: FDA_Inspections

> FDA Inspection 772787 for Omron Healthcare, Inc. on March 22, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 772787
- Company Name: Omron Healthcare, Inc.
- Inspection Date: 2012-03-22
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 772787 - 2012-03-22](https://www.keypedia.com/records/fda_inspections/omron-healthcare-inc/21eb10a4-69de-41e5-ad12-9d22555dddea)
- [FDA Inspection 731708 - 2011-05-13](https://www.keypedia.com/records/fda_inspections/omron-healthcare-inc/5da7bfcb-52ae-49e4-9e29-15849db24a78)

Company: https://www.keypedia.com/companies/omron-healthcare-inc/c110d68e-b6b6-4f81-a962-0fff593b0af2

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