# Kimberly-Clark Corporation – FDA Inspection, Jun 23, 2017

Source: https://www.keypedia.com/records/fda_inspections/kimberly-clark-corporation/edc5e5a8-5801-4354-9dbc-4c67cf69217c
Source feed: FDA_Inspections

> FDA inspection 1028989 of Kimberly-Clark Corporation, June 23, 2017. Form 483 issued. 3 other FDA inspections on record for this company.

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1028989
- Company Name: Kimberly-Clark Corporation
- Inspection Date: 2017-06-23
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Minneapolis District Office
- Citation Count: 0

## Related Documents

- [FDA Inspection 1097566 - 2019-07-25](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corporation/bdb7be0c-668e-46f9-92f0-0d92720fa347)
- FDA Inspection 864648 - 2014-01-30
- [FDA Inspection 778373 - 2012-06-08](https://www.keypedia.com/records/fda_inspections/kimberly-clark-corporation/b12b5460-a43b-491d-867d-b27e9ec6f03a)

Company: https://www.keypedia.com/companies/kimberly-clark-corporation/d1047438-8f53-4a80-b170-74c8e34d2c0c

Office: https://www.keypedia.com/offices/minneapolis-district-office/c79fc8dc-f884-48fc-ba80-2947f662511d