FDA inspection

Kimberly-Clark Corporation: FDA inspection ending Jun 8, 2012

FDA inspection 778373 · Voluntary Action Indicated (VAI) · Neenah, WI

Key facts

Inspection ID 778373
Firm Kimberly-Clark Corporation
FEI number 3003701733
Address 2100 Winchester Rd
City Neenah
State WI
ZIP 54956
Country United States
Fiscal year 2012
Inspection end date Jun 8, 2012
Classification Voluntary Action Indicated (VAI)
Project area Compliance: 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

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