Warning letter
General Electric Medical System: warning letter of Jul 27, 1997
FDA warning letter UCM065753 · Dallas District Office
Key facts
| Reference number | UCM065753 |
|---|---|
| Company | General Electric Medical System |
| Subject | Devices/X-ray Equipment |
| Issue date | Jul 27, 1997 |
| Posted date | Jul 27, 1997 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 1020.32, 1020, 1020.31, 1020.31(e)(3), 1020.31(e), 1020.32(a) |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: