Warning letter
Mainline Technology, Inc [ARCHIVED]: warning letter of Jan 23, 2009
FDA warning letter 44758 · Detroit District Office
Key facts
| Reference number | 44758 |
|---|---|
| Company | Mainline Technology, Inc [ARCHIVED] |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Jan 23, 2009 |
| Posted date | Jan 23, 2009 |
| Issuing office | Detroit District Office |
| Product type | Devices |
| CFR sections cited | 806, 806.2(d), 806.2(j), 820, 820.40, 806.10(a)(2), 806.10(b), 807.81(b) |
| Inspection city | Ann Arbor |
| Inspection ZIP | 48108-2219 |
| Inspection start date | Jul 15, 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: