FDA issued a Warning Letter to Kimberly-Clark Corporation on 8/8/2012 as a result of this inspection.
FDA investigators audited the Kimberly-Clark - Roswell, GA, United States facility and issued 1 inspectional observation (via FDA 483) on 28 Mar 2012.
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- Category: Medical Devices & Rad Health
- Number of Observations: 1
- Inspection end: 28 Mar 2012
- Location: Roswell, United States
- FEI: 1000015879