Warning letter
Diversified Manufacturing Corporation: warning letter of Oct 20, 2005
FDA warning letter UCM075650 · Minneapolis District Office
Key facts
| Reference number | UCM075650 |
|---|---|
| Company | Diversified Manufacturing Corporation |
| Subject | CGMP for Finished Pharmaceutical |
| Issue date | Oct 20, 2005 |
| Posted date | Oct 20, 2005 |
| Issuing office | Minneapolis District Office |
| Product type | Drugs |
| CFR sections cited | 211.192, 201.66, 211.166, 211.84(a), 211.137(a) |
| Country | 3 |
| Inspection city | Prescott |
| Inspection ZIP | 54021-1768 |
| Inspection start date | Mar 4, 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: