# Sysmex America, Inc. – FDA Inspection, Feb 6, 2012

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

> FDA inspection 769601 of Sysmex America, Inc., February 06, 2012. Classification: Voluntary Action Indicated (VAI). 6 citations under 21 CFR part 820. 1 other FDA inspection on record for this company.

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 769601
- Company Name: Sysmex America, Inc.
- Inspection Date: 2012-02-06
- 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

## Related Documents

- [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