Warning letter
Aros Surgical Instruments Corporation: warning letter of Sep 25, 2015
FDA warning letter 452629 · Los Angeles District Office
Key facts
| Reference number | 452629 |
|---|---|
| Company | Aros Surgical Instruments Corporation |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Sep 25, 2015 |
| Posted date | Oct 26, 2015 |
| Issuing office | Los Angeles District Office |
| Product type | Devices |
| CFR sections cited | 807.81(a)(3)(i), 820.40, 807.81(b), 820 |
| Inspection city | North Wales |
| Inspection ZIP | 19454 |
| Inspection start date | Feb 2, 2015 |
| Letter on fda.gov | web.archive.org |
At a glance
- 1–9 CFR sections cited
- VAI 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: