Warning letter
Hill-Rom, Inc.: warning letter of Mar 2, 2012
FDA warning letter 240334 · Detroit District Office
Key facts
| Reference number | 240334 |
|---|---|
| Company | Hill-Rom, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Mar 2, 2012 |
| Posted date | Mar 2, 2012 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3)(ii), 880.5100, 820, 820.40, 807.81(b), 880.5150 |
| Inspection city | Batesville |
| Inspection ZIP | 47006 |
| Inspection start date | Sep 20, 2011 |
| 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: