FDA Inspection 1319106 — ITW Filtertek

ITW Filtertek — FEI 1000034828

The FDA completed an inspection of ITW Filtertek on May 20, 2026 in Hebron, 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
May 20, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Hebron, IL (United States)