Warning letter
CORPAK MedSystems, Inc.: warning letter of Apr 10, 2013
FDA warning letter 393542 · Chicago District Office
Key facts
| Reference number | 393542 |
|---|---|
| Company | CORPAK MedSystems, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Apr 10, 2013 |
| Posted date | Apr 10, 2013 |
| Issuing office | Chicago District Office |
| Product type | Devices |
| CFR sections cited | 820, 803.50(a), 803, 803.3, 803.17, 803.52(f)(1) |
| Inspection city | Alpharetta |
| Inspection ZIP | 30004 |
| Inspection start date | Nov 26, 2012 |
| 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: