Warning letter
St. Joseph's Candler-Mobile Mammography: warning letter of Mar 12, 2007
FDA warning letter UCM076320 · Atlanta District Office
Key facts
| Reference number | UCM076320 |
|---|---|
| Company | St. Joseph's Candler-Mobile Mammography |
| Subject | Mammography Quality Standards |
| Issue date | Mar 12, 2007 |
| Posted date | Mar 12, 2007 |
| Issuing office | Atlanta District Office |
| Product type | Devices |
| CFR sections cited | 900.12(e)(1), 900.12(e)(2), 900.12(e)(7), 900.12(e)(9)(ii), 900.12(j) |
| Country | 3 |
| Inspection city | Savannah |
| Inspection ZIP | 31405-6015 |
| Inspection start date | Feb 5, 2007 |
| 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: