Warning letter
Bass Medical Inc [ARCHIVED]: warning letter of Feb 12, 2009
FDA warning letter 41740 · New Orleans District Office
Key facts
| Reference number | 41740 |
|---|---|
| Company | Bass Medical Inc [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Feb 12, 2009 |
| Posted date | Feb 12, 2009 |
| Issuing office | New Orleans District Office |
| Product type | Devices |
| CFR sections cited | 803, 803.17, 803.17(a)(1), 803.17(a)(2), 820 |
| Inspection city | Hoover |
| Inspection ZIP | 35244-4171 |
| Inspection start date | Sep 24, 2008 |
| 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: