# FDA Inspection 1015622 - Sysmex RA Co., LTD - April 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/sysmex-ra-co-ltd/1051ecbb-f45d-44be-8002-843c00a5a0b8
Source feed: FDA_Inspections

> FDA Inspection 1015622 for Sysmex RA Co., LTD on April 20, 2017. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1015622
- Company Name: Sysmex RA Co., LTD
- Inspection Date: 2017-04-20
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1015622 - 2017-04-20](https://www.keypedia.com/records/fda_inspections/sysmex-ra-co-ltd/ac88ab4e-0f05-4463-81ee-92d6c4a1b6a9)

Company: https://www.keypedia.com/companies/sysmex-ra-co-ltd/a1bc5101-f1c5-4744-acdb-8e5513655cf5

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