FDA Inspection 1199402 — Sysmex America, Inc.

Sysmex America, Inc. — FEI 3009711478

The FDA completed an inspection of Sysmex America, Inc. on March 2, 2023 in Lincolnshire, IL. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
March 2, 2023
Fiscal Year
2023
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Lincolnshire, IL (United States)