FDA Inspection 1097565 — Kimberly-Clark Corporation Cold Spring

Kimberly-Clark Corporation Cold Spring — FEI 1000139864

The FDA completed an inspection of Kimberly-Clark Corporation Cold Spring on July 25, 2019 in Neenah, WI. The inspection was classified NAI (No Action Indicated — no objectionable conditions were found). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI) (NAI)
End Date
July 25, 2019
Fiscal Year
2019
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
Neenah, WI (United States)

Citations

IDCFRDescription
328221 CFR 820.90(a)Nonconforming product, Lack of or inadequate procedures