# FDA Inspection 1097566 - Kimberly-Clark Corporation - July 25, 2019

Source: https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation/67f65dbc-c225-444c-aade-ad8f62ca3775
Source feed: FDA_Inspections

> FDA Inspection 1097566 for Kimberly-Clark Corporation on July 25, 2019. Classification: Voluntary Action Indicated (VAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1097566
- Company Name: Kimberly-Clark Corporation
- Inspection Date: 2019-07-25
- Classification: Voluntary Action Indicated (VAI)
- Project Area: Postmarket Assurance: Devices
- Product Type: Devices
- Office Name: Center for Devices and Radiological Health

## Related Documents

- [FDA Inspection 1097566 - 2019-07-25](https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation/bdb7be0c-668e-46f9-92f0-0d92720fa347)
- [FDA Inspection 864648 - 2014-01-30](https://www.globalkeysolutions.net/records/fda_inspections/kimberly-clark-corporation/a7446acb-924a-4da8-9677-34796cb2246e)
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Company: https://www.globalkeysolutions.net/companies/kimberly-clark-corporation/d1047438-8f53-4a80-b170-74c8e34d2c0c

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