# FDA Inspection 619285 - Kimberly- Clark Corp. - September 24, 2009

Source: https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/52f02723-14ce-45e9-827c-7a7bfb0c4cab
Source feed: FDA_Inspections

> FDA Inspection 619285 for Kimberly- Clark Corp. on September 24, 2009. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 619285
- Company Name: Kimberly- Clark Corp.
- Inspection Date: 2009-09-24
- Classification: No Action Indicated (NAI)
- Project Area: Compliance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 710835 - 2011-02-15](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/ad2f9445-f379-44f9-945e-e9b89121228e)
- [FDA Inspection 619285 - 2009-09-24](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/0dea34be-19f0-4864-92c0-0851869ba90d)

Company: https://www.keypedia.com/companies/kimberly-clark-corp/701f6e59-2e6d-48a4-8ffe-a639a20a4024

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