# Sysmex RA Co., LTD – FDA Inspection, Apr 20, 2017

Source: https://www.keypedia.com/records/fda_inspections/sysmex-ra-co-ltd/ac88ab4e-0f05-4463-81ee-92d6c4a1b6a9
Source feed: FDA_Inspections

> FDA inspection 1015622 of Sysmex RA Co., LTD, April 20, 2017. Classification: Voluntary Action Indicated (VAI). 5 citations under 21 CFR parts 803 and 820. Form 483 issued.

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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)
- 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: 5

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/frank-j-marciniak/6995351a-6afc-4056-9692-d4aeb711dd92)

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