Performance Health Supply LLC

FDA Regulatory Profile

Performance Health Supply LLC has 0 FDA recalls, 5 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Performance Health Supply LLC" and its spelling variant "Performance Health Supply".

Latest inspection
Apr 23, 2026 · NAI

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Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 8, 2026File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections5Nov 13, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

FDA record by year

Performance Health Supply LLC's FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Performance Health Supply LLC: FDA inspections per year 2017: 0 inspections020172018: 0 inspections020182019: 1 inspections120192020: 0 inspections020202021: 0 inspections020212022: 0 inspections020222023: 0 inspections020232024: 0 inspections020242025: 0 inspections020252026: 1 inspections12026
YearInspectionsOAIWarning lettersRecall recordsClass I
202610000
202500000
202400000
202300000
202200000
202100000
202000000
201910000
201800000
201700000

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

Recent FDA inspections

5 inspections from May 21, 2010 to Apr 23, 2026.

DateSiteProductClassificationFEI
Apr 23, 2026Indianapolis, INFood/CosmeticsNo Action Indicated (NAI)3013473968
Apr 17, 2019Cedarburg, WIDevicesVoluntary Action Indicated (VAI)2128677
Sep 18, 2012Brown Deer, WIDevicesNo Action Indicated (NAI)1048003
Apr 27, 2012Cedarburg, WIDevicesVoluntary Action Indicated (VAI)2128677
May 21, 2010Cedarburg, WIDevicesVoluntary Action Indicated (VAI)2128677
NAI
No objectionable conditions or practices were found during the inspection.
VAI
Objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action.
OAI
Regulatory and/or administrative actions are recommended.

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

3 inspected sites, newest inspection first.

FacilityLocationInspectionsLatest
FEI 3013473968Indianapolis, IN1Apr 23, 2026
FEI 2128677Cedarburg, WI3Apr 17, 2019
FEI 1048003Brown Deer, WI1Sep 18, 2012

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