FDA Inspection 843023 — KCI USA, Inc.

KCI USA, Inc. — FEI 3005178245

The FDA completed an inspection of KCI USA, Inc. on August 2, 2013 in San Antonio, TX. 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
August 2, 2013
Fiscal Year
2013
Product Type
Devices
Project Area
Compliance: Devices
Location
San Antonio, TX (United States)