Warning letter
Midmark Corporation [ARCHIVED]: warning letter of Dec 28, 2011
FDA warning letter 234874 · Cincinnati District Office
Key facts
| Reference number | 234874 |
|---|---|
| Company | Midmark Corporation [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Dec 28, 2011 |
| Posted date | Dec 28, 2011 |
| Issuing office | Cincinnati District Office |
| Product type | Devices |
| CFR sections cited | 803.17, 803, 803.3, 803.50, 803.53, 803.20(c)(1), 820, 803.50(b) |
| Inspection city | Versailles |
| Inspection ZIP | 45380 |
| Inspection start date | Aug 23, 2011 |
| 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: