Warning letter
ZIIP, Inc.: warning letter of May 22, 2026
FDA warning letter 725870 · Center for Devices and Radiological Health
Key facts
| Reference number | 725870 |
|---|---|
| Company | ZIIP, Inc. |
| Subject | CGMP/QSR/Medical Devices/Adulterated |
| Issue date | May 22, 2026 |
| Posted date | Jul 14, 2026 |
| Issuing office | Center for Devices and Radiological Health |
| Product type | Devices |
| CFR sections cited | 882.5890, 807.81(a)(1), 807.81(a)(3), 807.81(a)(3)(i), 807.81(b)(1)(i), 820, 882.1275 |
| Inspection city | Pleasant Hill |
| Inspection ZIP | 94523 |
| Inspection start date | Jan 5, 2026 |
| Letter on fda.gov | fda.gov |
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: