Warning letter
Delta Medical Center: warning letter of Sep 15, 2000
FDA warning letter UCM068854 · New Orleans District Office
Key facts
| Reference number | UCM068854 |
|---|---|
| Company | Delta Medical Center |
| Subject | Medical Devices/Lacks Medication & Device Experience Report/Misbranded |
| Issue date | Sep 15, 2000 |
| Posted date | Sep 15, 2000 |
| Issuing office | New Orleans District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 803, 803.30 |
| 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: