FDA Inspection 1275747 — SYSMEX AMERICA - Vernon Hills
The FDA completed an inspection of SYSMEX AMERICA - Vernon Hills on Jul 1, 2025 in Vernon Hills, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.
Inspection Details
- Classification
- No Action Indicated (NAI)
- End Date
- Jul 1, 2025
- Fiscal Year
- 2025
- Product Type
- Devices
- Project Area
- Postmarket Assurance: Devices
- Location
- Vernon Hills, IL (United States)