FDA inspection

KCI USA, Inc.: FDA inspection ending Aug 2, 2013

FDA inspection 843023 · No Action Indicated (NAI) · San Antonio, TX

Key facts

Inspection ID 843023
Firm KCI USA, Inc.
FEI number 3005178245
Address 6203 Farinon Dr
City San Antonio
State TX
ZIP 78249
Country United States
Fiscal year 2013
Inspection end date Aug 2, 2013
Classification No Action Indicated (NAI)
Project area Compliance: Devices
Product type Devices

At a glance

  • None Citations
  • None Posted citations
  • No Warning letter followed
  • No 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