FDA Inspection 646525 — RLS Interventional, Inc.

RLS Interventional, Inc. — FEI 3001237677

The FDA completed an inspection of RLS Interventional, Inc. on Feb 4, 2010 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
Feb 4, 2010
Fiscal Year
2010
Product Type
Devices
Project Area
Compliance: Devices
Location
Kentwood, MI (United States)

Sources: openFDA, FDA Data Dashboard, FDA.gov. Report a data issue: hello@regdatalab.com.