Warning letter
Arrowhead DE LLC, DBA Arrowhead Medical Device Technologies: warning letter of May 18, 2012
FDA warning letter 301261 · New Orleans District Office
Key facts
| Reference number | 301261 |
|---|---|
| Company | Arrowhead DE LLC, DBA Arrowhead Medical Device Technologies |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | May 18, 2012 |
| Posted date | May 18, 2012 |
| Issuing office | New Orleans District Office |
| Product type | Devices |
| CFR sections cited | 803, 820 |
| Inspection city | Peachtree City |
| Inspection ZIP | 30269 |
| Inspection start date | Feb 13, 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: