Warning letter
Eaton Manufacturing Corporation Dba Eaton Medical [ARCHIVED]: warning letter of Jul 27, 2010
FDA warning letter 119929 · New Orleans District Office
Key facts
| Reference number | 119929 |
|---|---|
| Company | Eaton Manufacturing Corporation Dba Eaton Medical [ARCHIVED] |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Jul 27, 2010 |
| Posted date | Jul 27, 2010 |
| Issuing office | New Orleans District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 820 |
| Inspection city | Memphis |
| Inspection ZIP | 38104 |
| Inspection start date | Jun 23, 2010 |
| 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: