# RESTECH, dba Mederi RF LLC – FDA Inspection, Sep 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 of RESTECH, dba Mederi RF LLC, September 18, 2024. Classification: No Action Indicated (NAI). 5 citations under 21 CFR part 820. Form 483 issued.

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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)
- Classification Code: NAI
- Project Area: Postmarket Assurance: Medical Devices
- Product Type: Medical Devices & Rad Health
- Center: Medical Devices & Rad Health
- Office Name: Dallas District Office
- Citation Count: 5

## Related Officers

- [Issuing Officer](https://www.keypedia.com/people/jocelyn-c-turner/7e39f6e0-9750-4460-8a4e-27ee9306b77e)

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