Warning letter
Danmar Product, Inc.: warning letter of Sep 6, 2007
FDA warning letter UCM076495 · Detroit District Office
Key facts
| Reference number | UCM076495 |
|---|---|
| Company | Danmar Product, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated/Misbranded |
| Issue date | Sep 6, 2007 |
| Posted date | Sep 6, 2007 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 807.20(a)(2), 820 |
| Country | 3 |
| Inspection city | Ann Arbor |
| Inspection ZIP | 48103-9104 |
| Inspection start date | Jun 1, 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: