Warning letter
Kimberly-Clark Corporation: warning letter of Aug 8, 2012
FDA warning letter 305878 · Atlanta District Office
Key facts
| Reference number | 305878 |
|---|---|
| Company | Kimberly-Clark Corporation |
| Subject | Devices/Misbranded |
| Issue date | Aug 8, 2012 |
| Posted date | Aug 8, 2012 |
| Issuing office | Atlanta District Office |
| Product type | Devices |
| CFR sections cited | 806, 806.20, 806.2(i) |
| Inspection city | Roswell |
| Inspection ZIP | 30076 |
| Inspection start date | Mar 20, 2012 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- OAI Linked inspection classification
- Yes Form FDA 483 issued
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About FDA warning letters
FDA warning letters notify a firm of significant regulatory violations found during an inspection or review and request prompt corrective action.
Source: U.S. Food and Drug Administration (FDA), Warning Letters · Source date: