# FDA Inspection 769601 - Sysmex America, Inc. - February 06, 2012

Source: https://www.keypedia.com/records/fda_inspections/sysmex-america-inc/caeeeaf2-e424-4893-a145-65d958e772a9
Source feed: FDA_Inspections

> FDA Inspection 769601 for Sysmex America, Inc. on February 06, 2012. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 769601
- Company Name: Sysmex America, Inc.
- Inspection Date: 2012-02-06
- 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 769601 - 2012-02-06](https://www.keypedia.com/records/fda_inspections/sysmex-america-inc/3a65f640-6cdb-4a6f-8ead-466664852938)
- [FDA Inspection 626786 - 2009-10-28](https://www.keypedia.com/records/fda_inspections/sysmex-america-inc/177b2c0b-360d-45a7-b832-af1ef89b6722)

Company: https://www.keypedia.com/companies/sysmex-america-inc/a58d187e-7c39-434e-9128-4837a184ae5f

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