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FDA Inspection
•RLS INTERVENTIONAL INC.•September 17, 2026

RLS INTERVENTIONAL INC. – FDA Inspection, Sep 17, 2026

Record Details

This FDA Inspection record concerns RLS INTERVENTIONAL INC., with an inspection on September 17, 2026, issued by the Center for Devices and Radiological Health, covering devices.

Company
RLS INTERVENTIONAL INC.
Inspection Date
September 17, 2026
Product Type
Devices
Office
Center for Devices and Radiological Health
View Company Profile

ID · 751c8b45-5076-4144-aef9-efff93aa8ab7

Inspection Facts

No Action Indicated (NAI)

No objectionable conditions or practices were found during the inspection.

Inspection number
1336044
Project area
Postmarket Assurance: Devices

FDA Citations

1
  1. 21 CFR 830GUDID Information required for unique device identification.

Full citation text and observation details available on the Dashboard.

Other FDA inspections of RLS INTERVENTIONAL INC.

4
DateClassificationOfficeProject area
March 18, 2014NAICenter for Devices and Radiological HealthCompliance: Devices
December 26, 2012NAICenter for Devices and Radiological HealthCompliance: Devices
October 6, 2011NAICenter for Devices and Radiological HealthCompliance: Devices
February 4, 2010NAICenter for Devices and Radiological HealthPostmarket Assurance: Devices
Other documents for RLS INTERVENTIONAL INC.
  • FDA Inspection 870420 - 2014-03-18
  • FDA Inspection 811998 - 2012-12-26
  • FDA Inspection 748918 - 2011-10-06
  • FDA Inspection 646525 - 2010-02-04

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