# FDA Inspection 984894 - Sysmex Reagents America, Inc. - June 07, 2016

Source: https://www.keypedia.com/records/fda_inspections/sysmex-reagents-america-inc/f2c1b869-712f-4cf2-b334-e1ddc2c61f4e
Source feed: FDA_Inspections

> FDA Inspection 984894 for Sysmex Reagents America, Inc. on June 07, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 984894
- Company Name: Sysmex Reagents America, Inc.
- Inspection Date: 2016-06-07
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 773199 - 2012-02-06](https://www.keypedia.com/records/fda_inspections/sysmex-reagents-america-inc/42981bd2-b945-4409-a1e8-d3e4b87beefc)
- [FDA Inspection 773199 - 2012-02-06](https://www.keypedia.com/records/fda_inspections/sysmex-reagents-america-inc/6b2d18bf-1624-44f2-9822-499760b9056f)

Company: https://www.keypedia.com/companies/sysmex-reagents-america-inc/42ccad2d-3cba-49aa-995f-28e3c6b0eab7

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