Warning letter
Guy & O'Neill Inc.: warning letter of Apr 2, 1999
FDA warning letter UCM067240 · Minneapolis District Office
Key facts
| Reference number | UCM067240 |
|---|---|
| Company | Guy & O'Neill Inc. |
| Subject | Good Manufacturing Practices Violations |
| Issue date | Apr 2, 1999 |
| Posted date | Apr 2, 1999 |
| Issuing office | Minneapolis District Office |
| Product type | Unknown |
| CFR sections cited | 211.137, 2, 21, 211, 211.103, 211.160(b) |
| 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: