483
Kimberly-Clark CorporationFDA 483 - Kimberly-Clark Corporation
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Record Details
This FDA Form 483 inspection report for Kimberly-Clark Corporation did not cite any observations. The inspection found no deficiencies requiring corrective action, indicating compliance with regulatory standards.
- Company
- Kimberly-Clark Corporation
- Product Type
- Device
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ID · 82731398-bc5b-4b09-91e0-f99eec55f938