# FDA Inspection 990227 - SYSMEX CORPORATION I-SQUARE - September 16, 2016

Source: https://www.keypedia.com/records/fda_inspections/sysmex-corporation-i-square/3ec41a48-e88d-4fcf-9b6c-ef749f4e7882
Source feed: FDA_Inspections

> FDA Inspection 990227 for SYSMEX CORPORATION I-SQUARE on September 16, 2016. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 990227
- Company Name: SYSMEX CORPORATION I-SQUARE
- Inspection Date: 2016-09-16
- 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 990227 - 2016-09-16](https://www.keypedia.com/records/fda_inspections/sysmex-corporation-i-square/7f53dbf7-7757-49ff-92c8-6bea3514a76a)

Company: https://www.keypedia.com/companies/sysmex-corporation-i-square/d792121c-b6fc-4b05-b8bf-cd84b4dd965f

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