Warning letter
Diagnostic Imaging: warning letter of Mar 3, 2000
FDA warning letter UCM068183 · Dallas District Office
Key facts
| Reference number | UCM068183 |
|---|---|
| Company | Diagnostic Imaging |
| Subject | Performance Standards for Diagnostic X-ray Equipment |
| Issue date | Mar 3, 2000 |
| Posted date | Mar 3, 2000 |
| Issuing office | Dallas District Office |
| Product type | Devices |
| CFR sections cited | 1020.32(a), 1020, 1020.31, 1020.31(g) |
| 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: