Murphy USA 8842 — FDA Facility Profile

FEI 3038684031

Murphy USA 8842 (FEI 3038684031) located in Little Rock, AR, United States has FDA compliance records.

Reviewing Murphy USA 8842 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 Murphy USA 8842 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
1 listed by FDA for this FEI, latest Jul 10, 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
Little Rock, AR (United States)

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