Warning letter
Lifecore Biomedical, Inc.: warning letter of Oct 8, 2004
FDA warning letter UCM146908 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM146908 |
|---|---|
| Company | Lifecore Biomedical, Inc. |
| Subject | Medical Device Reporting/Misbranded |
| Issue date | Oct 8, 2004 |
| Posted date | Oct 8, 2004 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 803, 803.20, 803.3(bb)(1), 803.50(a)(1), 803.50(a)(2), 803.3(bb), 803.20(c)(2), 803.50(a) |
| Country | 3 |
| Inspection city | Chaska |
| Inspection ZIP | 55318-3051 |
| Inspection start date | Apr 29, 2004 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- VAI 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: