Warning letter
Ferno-Washington, Inc: warning letter of Apr 7, 2006
FDA warning letter UCM075862 · Cincinnati District Office
Key facts
| Reference number | UCM075862 |
|---|---|
| Company | Ferno-Washington, Inc |
| Subject | Current Good Manufacturing Practice/Medical Device Report Regulation/Adulterated |
| Issue date | Apr 7, 2006 |
| Posted date | Apr 7, 2006 |
| Issuing office | Cincinnati District Office |
| Product type | Devices |
| CFR sections cited | 806.10(a)(1), 820, 803, 803.17, 806, 803.17(a)(1), 803.18(b)(1)(i), 803.50(a)(2) |
| Country | 3 |
| Inspection city | Wilmington |
| Inspection ZIP | 45177-9371 |
| Inspection start date | Sep 26, 2005 |
| 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: