Warning letter
Sage Products Inc [ARCHIVED]: warning letter of Jan 22, 2009
FDA warning letter 28947 · Chicago District Office
Key facts
| Reference number | 28947 |
|---|---|
| Company | Sage Products Inc [ARCHIVED] |
| Subject | CGMP Manufacturer, Processsing, Packing, Holding Drugs/Devices/Adulterated |
| Issue date | Jan 22, 2009 |
| Posted date | Jan 22, 2009 |
| Issuing office | Chicago District Office |
| Product type | Drugs |
| CFR sections cited | 820, 211.160(b), 211.180(e), 820.1 |
| Inspection city | Cary |
| Inspection ZIP | 60013-1804 |
| Inspection start date | Jun 2, 2008 |
| 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: