# FDA Warning Letter: LEEL Tech
> 2024-08-28 · Center for Devices and Radiological Health · `e0fe3a53f40ca839`
## Letter
- **Company:** LEEL Tech
- **Posted Date:** 2024-08-28
- **Letter Issue Date:** 2024-08-07
- **Issuing Office:** Center for Devices and Radiological Health
## Subject
Investigational Device Exemptions (IDE)/Premarket Approval Application (PMA) Adulterated Device
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*Source: [FDA Warning Letters](https://www.fda.gov/inspections-compliance-enforcement-and-criminal-investigations/compliance-actions-and-activities/warning-letters) · AI Analytics · CC0 1.0*