FDA Inspection 720291 — Kimberly-Clark Corporation Cold Spring

Kimberly-Clark Corporation Cold Spring — FEI 1000139864

The FDA completed an inspection of Kimberly-Clark Corporation Cold Spring on March 2, 2011 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
March 2, 2011
Fiscal Year
2011
Product Type
Devices
Project Area
Compliance: Devices
Location
Neenah, WI (United States)