FDA Inspection
Kimberly-Clark CorporationKimberly-Clark Corporation – FDA Inspection, Jun 23, 2017
Record Details
This FDA Inspection record concerns Kimberly-Clark Corporation, with an inspection on June 23, 2017, issued by the Minneapolis District Office, covering medical devices & rad health.
- Company
- Kimberly-Clark Corporation
- Inspection Date
- June 23, 2017
- Product Type
- Medical Devices & Rad Health
View Company Profile
ID · edc5e5a8-5801-4354-9dbc-4c67cf69217c
Inspection Facts
- Inspection number
- 1028989
- FDA center
- Medical Devices & Rad Health
- Outcome
- Form 483 issued
Other FDA inspections of Kimberly-Clark Corporation
3| Date | Classification | Office | Project area |
|---|---|---|---|
| July 25, 2019 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
| January 30, 2014 | NAI | Center for Devices and Radiological Health | Compliance: Devices |
| June 8, 2012 | VAI | Center for Devices and Radiological Health | Compliance: Devices |
Other documents for Kimberly-Clark Corporation
- FDA Inspection 1097566 - 2019-07-25
- FDA Inspection 864648 - 2014-01-30
- FDA Inspection 778373 - 2012-06-08
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