FDA inspection

Kimberly-Clark Corporation Cold Spring: FDA inspection ending Jul 25, 2019

FDA inspection 1097565 · Voluntary Action Indicated (VAI) · Neenah, WI

Key facts

Inspection ID 1097565
Firm Kimberly-Clark Corporation Cold Spring
FEI number 1000139864
Address 1050 Cold Spring Rd
City Neenah
State WI
ZIP 54956
Country United States
Fiscal year 2019
Inspection end date Jul 25, 2019
Classification Voluntary Action Indicated (VAI)
Project area Postmarket Assurance: Devices
Product type Devices

At a glance

  • 1–9 Citations
  • 1–9 Posted citations
  • No Warning letter followed
  • Yes Form FDA 483 issued
  • No Establishment inspection report (EIR) exists
  • 1–9 Inspections at this FEI

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

About FDA inspections

FDA inspections are classified as No Action Indicated (NAI), Voluntary Action Indicated (VAI) or Official Action Indicated (OAI). Inspections of individual clinical investigators are not published here.

Source: U.S. Food and Drug Administration (FDA), inspection classification data

Browse all FDA inspections