Warning letter
American I.V. Products, Inc.: warning letter of Oct 19, 2005
FDA warning letter UCM075647 · Baltimore District Office
Key facts
| Reference number | UCM075647 |
|---|---|
| Company | American I.V. Products, Inc. |
| Subject | CGMP Requirement of the Quality System Regulation for Medical Device |
| Issue date | Oct 19, 2005 |
| Posted date | Oct 19, 2005 |
| Issuing office | Baltimore District Office |
| Product type | Devices |
| CFR sections cited | 820 |
| Country | 3 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
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: