Home / Facilities / 3013731989

QuikTrip — FDA Facility Profile

FEI 3013731989

QuikTrip (FEI 3013731989) located in Olathe, KS, United States has FDA compliance records.

Reviewing QuikTrip as a supplier? Request a free FDA snapshot: name up to five suppliers and get a PDF of their public FDA record, with sources and dates. You do not need an API connection. Each snapshot is prepared by hand.

Check this supplier

Or check QuikTrip yourself in Claude, Cursor or ChatGPT: get the full FDA risk summary, with inspections, warning letters, Form 483s and import alerts by site.

Get a free API key

What FDA found at this site

Inspections on record
None in FDA's published inspection data
Warning letters
2 listed by FDA for this FEI, latest Sep 30, 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.