# FDA Inspection 914417 - Kimberly-Clark Corp - February 12, 2015

Source: https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/a071d904-4926-4790-a7f6-538eaaa49a65
Source feed: FDA_Inspections

> FDA Inspection 914417 for Kimberly-Clark Corp on February 12, 2015. Classification: No Action Indicated (NAI).

---

## Details

- Record Type: FDA Inspection
- Inspection ID: 914417
- Company Name: Kimberly-Clark Corp
- Inspection Date: 2015-02-12
- 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 1062006 - 2018-06-13](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/f6ce5e65-7f61-46b5-98e8-348004ac4153)
- [FDA Inspection 914417 - 2015-02-12](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/3203253c-c86b-426b-a347-21b5046e2b58)
- [FDA Inspection 846219 - 2013-08-29](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corp/0892b66d-c81f-4dfb-bc84-fd7a7b30086f)

Company: https://www.keypedia.com/companies/kimberly-clark-corp/de7c6042-8f9c-4d8a-9202-85069ad22b13

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