FDA Inspection 1336044 — RLS Interventional, Inc.

RLS Interventional, Inc. — FEI 3001237677

The FDA completed an inspection of RLS Interventional, Inc. on Sep 17, 2026 in Kentwood, MI. The inspection was classified VAI (Voluntary Action Indicated — objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action). 1 citation was issued during this inspection. Product area: Devices.

Inspection Details

Classification
Voluntary Action Indicated (VAI)
End Date
Sep 17, 2026
Fiscal Year
2026
Product Type
Devices
Project Area
Compliance: Devices
Location
Kentwood, MI (United States)

Citations

IDCFRDescription
2280121 CFR 830.310(b)GUDID Information required for unique device identification.

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