Warning letter
Pulse Biomedical, Inc.: warning letter of Jul 30, 2007
FDA warning letter UCM076458 · Philadelphia District Office
Key facts
| Reference number | UCM076458 |
|---|---|
| Company | Pulse Biomedical, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | Jul 30, 2007 |
| Posted date | Jul 30, 2007 |
| Issuing office | Philadelphia District Office |
| Product type | Devices |
| CFR sections cited | 820, 820.40, 807.81(b) |
| Country | 3 |
| Inspection city | King Of Prussia |
| Inspection ZIP | 19406-2145 |
| Inspection start date | Feb 9, 2007 |
| 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: