Warning letter
Clearwater Products, LLC [ARCHIVED]: warning letter of Mar 10, 2010
FDA warning letter 85226 · Florida District Office
Key facts
| Reference number | 85226 |
|---|---|
| Company | Clearwater Products, LLC [ARCHIVED] |
| Subject | Medical Devices/Adulterated/Misbranded |
| Issue date | Mar 10, 2010 |
| Posted date | Mar 10, 2010 |
| Issuing office | Florida District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 820, 807.81(b) |
| Inspection city | Kennesaw |
| Inspection ZIP | 30144 |
| Inspection start date | Aug 24, 2009 |
| 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: