# FDA Inspection 1023356 - KCI USA, Inc. - April 21, 2017

Source: https://www.keypedia.com/records/fda_inspections/kci-usa-inc/0b9b9074-0a82-4e36-aa55-29f3d8fa41cf
Source feed: FDA_Inspections

> FDA Inspection 1023356 for KCI USA, Inc. on April 21, 2017. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1023356
- Company Name: KCI USA, Inc.
- Inspection Date: 2017-04-21
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1023356 - 2017-04-21](https://www.keypedia.com/records/fda_inspections/kci-usa-inc/45d91fc7-029b-493a-84df-297ee5a17ab6)
- [FDA Inspection 843023 - 2013-08-02](https://www.keypedia.com/records/fda_inspections/kci-usa-inc/f0568dc3-ae3a-4e6b-88a6-63e50a0faafb)
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- [FDA Inspection 784517 - 2012-05-01](https://www.keypedia.com/records/fda_inspections/kci-usa-inc/6d180f76-477d-4f74-97c0-662b5c366ee6)

Company: https://www.keypedia.com/companies/kci-usa-inc/5e570ec8-5c50-46ff-8604-28016a7cda54

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