FDA Inspection 965792 — Henkel US Operations Corporation

Henkel US Operations Corporation — FEI 3003940942

The FDA completed an inspection of Henkel US Operations Corporation on Apr 1, 2016 in Bedford Park, 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
Apr 1, 2016
Fiscal Year
2016
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Bedford Park, IL (United States)