FDA Inspection 773199 — Sysmex Reagents America, Inc.

Sysmex Reagents America, Inc. — FEI 3006949423

The FDA completed an inspection of Sysmex Reagents America, Inc. on Feb 6, 2012 in Mundelein, IL. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Feb 6, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Compliance: Devices
Location
Mundelein, IL (United States)

Citations

IDCFRDescription
323921 CFR 820.72(b)Remedial action - documentation