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Quiktrip 206 — FDA Facility Profile

FEI 3039669065

Quiktrip 206 (FEI 3039669065) located in Olathe, KS, United States has FDA compliance records.

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What FDA found at this site

Inspections on record
None in FDA's published inspection data
Warning letters
1 listed by FDA for this FEI, latest Sep 23, 2025

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.

Facility details

Location
Olathe, KS (United States)

Compliance actions

FDA data resources

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