Friona Industries LP

FDA Regulatory Profile

Friona Industries LP has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

Latest inspection
Sep 15, 2026 · NAI

Reviewing Friona Industries LP 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 Friona Industries LP 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

Summary

Record counts and when each FDA source was last refreshed
RecordsCountLast refreshedSource as ofStatus
Recalls0Nov 4, 2026 (checked Nov 8, 2026, unchanged)File dated Nov 3, 2026Current
510(k) clearances0Nov 8, 2026File dated Nov 2, 2026Current
Inspections9Nov 10, 2026Newest record Nov 5, 2026Current
Compliance actions0Nov 2, 2026Newest record Oct 29, 2026Current

Related names

NameRecalls510(k)InspectionsComplianceMost recent recall
Friona Industries, L.P., Limited Partnership
Same company group
0020—

Recent FDA Inspections

DateSiteProductClassificationFEI
Sep 15, 2026Satanta, KSVeterinaryNo Action Indicated (NAI)1930979
Sep 15, 2026Sublette, KSVeterinaryNo Action Indicated (NAI)1950216
Aug 12, 2025Satanta, KSVeterinaryNo Action Indicated (NAI)1930979
Aug 17, 2022Amarillo, TXVeterinaryNo Action Indicated (NAI)1619867
Apr 20, 2017Amarillo, TXVeterinaryNo Action Indicated (NAI)1619867
Oct 22, 2015Bovina, TXVeterinaryNo Action Indicated (NAI)1642714
May 22, 2012Amarillo, TXVeterinaryNo Action Indicated (NAI)1619867
Feb 27, 2012Bovina, TXVeterinaryNo Action Indicated (NAI)1642714
Sep 15, 2009Amarillo, TXVeterinaryNo Action Indicated (NAI)1619867

NAI means no objectionable conditions or practices were found during the inspection. VAI means objectionable conditions or practices were found, but the agency is not prepared to take or recommend any administrative or regulatory action. OAI means regulatory and/or administrative actions are recommended.

FDA-Inspected Facilities

FacilityLocationInspectionsLatest
FEI 1930979Satanta, KS2Sep 15, 2026
FEI 1950216Sublette, KS1Sep 15, 2026
FEI 1619867Amarillo, TX4Aug 17, 2022
FEI 1642714Bovina, TX2Oct 22, 2015

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