# FDA Inspection 1275747 - SYSMEX AMERICA - Vernon Hills - July 01, 2025

Source: https://www.keypedia.com/records/fda_inspections/sysmex-america-vernon-hills/26dcb187-68a8-42ed-8c1e-25c771650e2a
Source feed: FDA_Inspections

> FDA Inspection 1275747 for SYSMEX AMERICA - Vernon Hills on July 01, 2025. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1275747
- Company Name: SYSMEX AMERICA - Vernon Hills
- Inspection Date: 2025-07-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1275747 - 2025-07-01](https://www.keypedia.com/records/fda_inspections/sysmex-america-vernon-hills/e8e2c544-8100-426d-bf6f-712a0ef66b37)
- [FDA Inspection 1275747 - 2025-07-01](https://www.keypedia.com/records/fda_inspections/sysmex-america-vernon-hills/6da37d78-c81b-44e6-93da-2d8c6aa73312)

Company: https://www.keypedia.com/companies/sysmex-america-vernon-hills/3a7fa812-a178-4bc9-a22c-fbd0193aa481

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