Warning letter
Suretec Innovations, LLC: warning letter of Aug 13, 2026
FDA warning letter 730122 · Center for Drug Evaluation and Research (CDER)
Key facts
| Reference number | 730122 |
|---|---|
| Company | Suretec Innovations, LLC |
| Subject | CGMP/Finished Pharmaceuticals/Adulterated and Misbranded |
| Issue date | Aug 13, 2026 |
| Posted date | Aug 18, 2026 |
| Issuing office | Center for Drug Evaluation and Research (CDER) |
| Product type | Drugs |
| CFR sections cited | 207, 207.41(c)(1), 211.22, 211.22(d), 211.25(c), 211.34, 211.84(d)(1), 211.100(a), 211.165(b), 211.166(a), 211.192 |
| Inspection city | Gilbert |
| Inspection ZIP | 85233 |
| Inspection start date | Mar 2, 2026 |
| Letter on fda.gov | fda.gov |
At a glance
- 10–99 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: