Warning letter
AP Diagnostic Imaging, Inc.: warning letter of Oct 30, 2002
FDA warning letter UCM145272 · New Jersey District Office
Key facts
| Reference number | UCM145272 |
|---|---|
| Company | AP Diagnostic Imaging, Inc. |
| Subject | Mammography Quality Standards |
| Issue date | Oct 30, 2002 |
| Posted date | Oct 30, 2002 |
| Issuing office | New Jersey District Office |
| Product type | Devices |
| CFR sections cited | 900.12(c), 900.12(e), 900.12(e)(2), 900, 900.12(h), 900.12, 900.12(a) |
| Country | 3 |
| Inspection city | Edison |
| Inspection ZIP | 08820 |
| Inspection start date | Sep 16, 2002 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- 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: