Warning letter
Nelson Laboratories, Inc.: warning letter of Dec 21, 2004
FDA warning letter UCM146936 · Center for Devices and Radiological Health
Key facts
| Reference number | UCM146936 |
|---|---|
| Company | Nelson Laboratories, Inc. |
| Subject | Good Laboratory Practices |
| Issue date | Dec 21, 2004 |
| Posted date | Dec 21, 2004 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 58.31, 58.29(b), 58.35(a), 58.35(b)(1), 58.35(b)(3), 58.35(b)(4), 58.63(c), 58.81(a), 58.130(e) |
| Country | 3 |
| Inspection city | Salt Lake City |
| Inspection ZIP | 84123-6600 |
| Inspection start date | Jul 21, 2004 |
| 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: