FDA Inspection 811513 — Kimberly-Clark Corporation

Kimberly-Clark Corporation — FEI 1000015879

The FDA completed an inspection of Kimberly-Clark Corporation on November 7, 2012 in Roswell, GA. 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
November 7, 2012
Fiscal Year
2013
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Roswell, GA (United States)