# FDA Inspection 780239 - KCI USA, Inc. - May 01, 2012

Source: https://www.keypedia.com/records/fda_inspections/kci-usa-inc/7fa2e35c-5d50-4883-a171-b36c365dbf6b
Source feed: FDA_Inspections

> FDA Inspection 780239 for KCI USA, Inc. on May 01, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 780239
- Company Name: KCI USA, Inc.
- Inspection Date: 2012-05-01
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 780239 - 2012-05-01](https://www.keypedia.com/records/fda_inspections/kci-usa-inc/183ed1f8-14ca-4490-8466-5e937b70a4df)

Company: https://www.keypedia.com/companies/kci-usa-inc/fd7e1863-e130-4ca0-b825-87dd7b1ddeee

Office: https://www.keypedia.com/offices/center-for-devices-and-radiological-health/9d89aff6-e435-4764-87be-f58c01aca7f7