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RESOUNDANT, INC. — FDA Facility Profile

FEI 3013695852

RESOUNDANT, INC. is an FDA-registered facility (FEI 3013695852) located in Rochester, MN, US. RegDataLab tracks 2 FDA inspections at this facility.

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What FDA found at this site

Latest inspection
Apr 15, 2026: No Action Indicated (NAI)
Inspections on record
2 (2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name

A Form 483 lists an inspector's observations. OAI means FDA recommends regulatory and/or administrative action. A warning letter is FDA's formal enforcement notice. No record here does not establish that a site is safe. Check this site on FDA's Data Dashboard.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

DateResultWhat FDA cited
Apr 15, 2026No Action Indicated (NAI)No citations listed
Jul 20, 2022No Action Indicated (NAI)No citations listed

Facility details

Company
Resoundant Inc.
Location
Rochester, MN (US)
Source
device

FDA data resources

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