FDA Inspection 784517 — KCI USA, Inc.

KCI USA, Inc. — FEI 3005178245

The FDA completed an inspection of KCI USA, Inc. on May 1, 2012 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
May 1, 2012
Fiscal Year
2012
Product Type
Devices
Project Area
Postmarket Assurance: Devices
Location
San Antonio, TX (United States)