# FDA Inspection 1040298 - Sysmex America, Inc. - January 31, 2018

Source: https://www.keypedia.com/records/fda_inspections/sysmex-america-inc/5a406357-a55c-4a15-84ee-301bf1b61a49
Source feed: FDA_Inspections

> FDA Inspection 1040298 for Sysmex America, Inc. on January 31, 2018. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1040298
- Company Name: Sysmex America, Inc.
- Inspection Date: 2018-01-31
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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Company: https://www.keypedia.com/companies/sysmex-america-inc/ff0e1b31-714e-49f4-9eee-99a3851c859e

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