# FDA Inspection 1249477 - RESTECH, dba Mederi RF LLC - September 18, 2024

Source: https://www.keypedia.com/records/fda_inspections/restech-dba-mederi-rf-llc/8857019a-3d93-43c0-9bee-5dac2f4e4e27
Source feed: FDA_Inspections

> FDA Inspection 1249477 for RESTECH, dba Mederi RF LLC on September 18, 2024. Classification: No Action Indicated (NAI).

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## Details

- Record Type: FDA Inspection
- Inspection ID: 1249477
- Company Name: RESTECH, dba Mederi RF LLC
- Inspection Date: 2024-09-18
- Classification: No Action Indicated (NAI)
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Office Name: Dallas District Office

## Related Documents

- [FDA Inspection 1249477 - 2024-09-18](https://www.keypedia.com/records/fda_inspections/restech-dba-mederi-rf-llc/e2832ff1-1408-43a8-9973-b3aea0db3083)
- [FDA Inspection 1249477 - 2024-09-18](https://www.keypedia.com/records/fda_inspections/restech-dba-mederi-rf-llc/30407cfe-6f78-4a44-b0d7-c07142346f8e)
- [FDA Inspection 1249477 - 2024-09-18](https://www.keypedia.com/records/fda_inspections/restech-dba-mederi-rf-llc/433f32d6-6cb5-4c84-b564-fe3f98d289e6)

Company: https://www.keypedia.com/companies/restech-dba-mederi-rf-llc/2bfe885a-9927-4ae0-a1e3-7fd3efd9e220

Office: https://www.keypedia.com/offices/dallas-district-office/2d1ee9ae-c44c-4494-8186-a920a69b98f9