FDA Inspection 864648 — Kimberly-Clark Corporation

Kimberly-Clark Corporation — FEI 3003701733

The FDA completed an inspection of Kimberly-Clark Corporation on January 30, 2014 in Neenah, WI. 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
January 30, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Neenah, WI (United States)