# FDA Inspection 773923 - KCI MANUFACTURING - February 23, 2012

Source: https://www.keypedia.com/records/fda_inspections/kci-manufacturing/e7673778-7eeb-4997-b6eb-e20bd8448f4d
Source feed: FDA_Inspections

> FDA Inspection 773923 for KCI MANUFACTURING on February 23, 2012. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 773923
- Company Name: KCI MANUFACTURING
- Inspection Date: 2012-02-23
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

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- [FDA Inspection 917044 - 2015-02-05](https://www.keypedia.com/records/fda_inspections/kci-manufacturing/759a4a40-c03f-470a-90ee-af09898c5613)

Company: https://www.keypedia.com/companies/kci-manufacturing/df5fe130-cee1-4ac3-b4e2-fbda4ab78695

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