FDA Inspection 870420 — RLS Interventional, Inc.

RLS Interventional, Inc. — FEI 3001237677

The FDA completed an inspection of RLS Interventional, Inc. on Mar 18, 2014 in Kentwood, MI. The inspection was classified NAI (No Action Indicated — no objectionable conditions or practices were found during the inspection). Product area: Devices.

Inspection Details

Classification
No Action Indicated (NAI)
End Date
Mar 18, 2014
Fiscal Year
2014
Product Type
Devices
Project Area
Compliance: Devices
Location
Kentwood, MI (United States)

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