# Sysmex Corporation – FDA Inspection, Dec 8, 2016

Source: https://www.keypedia.com/records/fda_inspections/sysmex-corporation/38a3bef3-511f-48af-8945-a1ac89a44d0a
Source feed: FDA_Inspections

> FDA inspection 996934 of Sysmex Corporation, December 08, 2016. Classification: Voluntary Action Indicated (VAI). 1 citation under 21 CFR part 820. Form 483 issued.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 996934
- Company Name: Sysmex Corporation
- Inspection Date: 2016-12-08
- Classification: Voluntary Action Indicated (VAI)
- Classification Code: VAI
- Project Area: Compliance: Devices
- Product Type: Devices
- Center: Medical Devices & Rad Health
- Office Name: Center for Devices and Radiological Health
- Citation Count: 1

## Related Officers

- [Company Rep](https://www.keypedia.com/people/stephen-d-eich/a932e816-cbe3-4f1c-84e7-8a81cc8b529e)

Company: https://www.keypedia.com/companies/sysmex-corporation/060c3b5f-d084-406d-857a-7eddb248fbb3

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