Warning letter
Hill-Rom, Inc.: warning letter of Jan 15, 2008
FDA warning letter UCM1048431 · Detroit District Office
Key facts
| Reference number | UCM1048431 |
|---|---|
| Company | Hill-Rom, Inc. |
| Subject | CGMP/QSR/Medical Device Reporting/Adulterated/Misbranded |
| Issue date | Jan 15, 2008 |
| Posted date | Jan 15, 2008 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 7.3(m)(2), 803, 806, 803.50(a)(2), 806.10(a)(1), 820, 803.50(a), 806.10(a), 806.10(b) |
| Country | 3 |
| Inspection city | Batesville |
| Inspection ZIP | 47006-7520 |
| Inspection start date | May 29, 2007 |
| 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: