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Rangen, LLC FDA Inspection Record

FEI 3016448 · Inspections, Form 483s, warning letters and import refusals

Rangen, LLC is an FDA-inspected facility (FEI 3016448) located in Buhl, ID, US. RegDataLab tracks 7 FDA inspections and 1 compliance action at this facility.

What FDA found at this site

Latest inspection: Dec 7, 2023: No Action Indicated (NAI)
Inspections on record: 7 (1 OAI, 4 VAI, 2 NAI)
Last OAI inspection: Jun 11, 2009
Warning letters: 1 listed by FDA for this FEI, latest Feb 16, 2010
Recalls as the recalling firm: 2, latest Jun 12, 2007

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.

Inspections and what FDA cited

Newest first. Citations are the inspector observations FDA publishes for the inspection.

Date	Result	What FDA cited
Dec 7, 2023	No Action Indicated (NAI)	No citations listed
Jul 29, 2021	No Action Indicated (NAI)	No citations listed
Mar 1, 2018	Voluntary Action Indicated (VAI)	First batch assay (21 CFR 225.58(b)(1)) Adequate procedures established (21 CFR 225.42(b))
Nov 19, 2014	Voluntary Action Indicated (VAI)	Flush material handling (21 CFR 225.65(b)(2))
Apr 4, 2011	Voluntary Action Indicated (VAI)	Three assays per year (21 CFR 225.58(b)(1)) Flush material handling (21 CFR 225.65(b)(2)) Sequential production (21 CFR 225.65(b)(3)) Distribution record elements (21 CFR 225.110(b)(1)) and 1 more
Jul 9, 2010	Voluntary Action Indicated (VAI)	Assay results out of specification (21 CFR 225.58(d)) Distribution discontinued and control procedures established (21 CFR 225.58(e)) Subsequent production (21 CFR 225.58(e))
Jun 11, 2009	Official Action Indicated (OAI)	Protein blenders, feed manufacturers, distributors (21 CFR 589.2000(d)(1)) Separate equipment and facilities or adequate cleanout (21 CFR 589.2000(e)(1)) Written product separation procedures (21 CFR 589.2000(e)(1))

Recalls

Newest first. Recalls FDA's Enforcement Report lists with this FEI as the recalling firm. The recalling firm is not always the site that made the product. Search FDA's Enforcement Report by recall number.

Date	Class	Recall	Product and reason
Jun 12, 2007	Class III	V-375-2007	Aquaculture feeds labeled as being manufactured by Rangen, Buhl, ID. Products are sold in… and 26 more products Firm received binder (Aqua Tec II) that was contaminated with melamine (unapproved feed additive) from another manufacturer and…
Feb 13, 2007	Class II	V-025-2007	Custom dairy premix products: MNM ALL PURPOSE Pellet, HILLSIDE/CDL Prot-Buffer Meal, LEE… Products manufactured from bulk feed containing blood meal that was cross contaminated with prohibited meat and bone meal and the labeling…

FDA record score

2 of 100. A count of this site's adverse public FDA records, weighted by how recent each one is. A higher number means more, or more recent, records. Each record below adds the points shown.

Counted on Nov 14, 2026, method version 1. It counts records and does not judge the site: a low number does not establish that a site is safe, and sites that FDA inspects more often can collect more points. How this is counted.

7 records behind this number

Record	Date	Points x age weight	Adds
Inspection classified VAI	Mar 1, 2018	6 x 0.25	1.5
Inspection classified VAI	Nov 19, 2014	10 years or older, so it adds no points	0
Inspection classified VAI	Apr 4, 2011	10 years or older, so it adds no points	0
Inspection classified VAI	Jul 9, 2010	10 years or older, so it adds no points	0
Warning letter on FDA's dashboard, which does not show close-outs	Feb 16, 2010	10 years or older, so it adds no points	0
Inspection classified OAI	Jun 11, 2009	10 years or older, so it adds no points	0
Class II recall V-025-2007, this FEI as the recalling firm	Feb 13, 2007	10 years or older, so it adds no points	0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
Records	Last refreshed	Source as of	Status
Inspections	Nov 14, 2026	Newest record Nov 5, 2026	Current
Inspection citations	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions (warning letters, injunctions and other action types)	Nov 2, 2026	Newest record Oct 29, 2026	Current
Warning letter text	Nov 14, 2026	Newest record Nov 10, 2026	Current
Recalls (Enforcement Report)	Nov 14, 2026	Newest record Nov 11, 2026	Current
Form 483s and inspection documents	Nov 13, 2026	Newest record Nov 12, 2026	Current
Import refusals	Nov 2, 2026	Newest record Oct 22, 2026	Current

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Facility details

Company: Rangen, LLC
Location: Buhl, ID (US)
Source: inspections