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Ochoa's Queseria LLC FDA Inspection Record

FEI 3008627958 · Inspections, Form 483s, warning letters and import refusals

Ochoa's Queseria LLC is an FDA-inspected facility (FEI 3008627958) located in Salem, OR, US. RegDataLab tracks 6 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 17, 2025: No Action Indicated (NAI)
Inspections on record
6 (4 VAI, 2 NAI)
Last OAI inspection
None on record
Warning letters
None matched to this FEI. Many letters do not state an FEI: search warning letters by company name
Recalls as the recalling firm
3, latest Aug 20, 2018

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.

DateResultWhat FDA cited
Mar 17, 2025No Action Indicated (NAI)No citations listed
Jun 30, 2022No Action Indicated (NAI)No citations listed
Sep 26, 2019Voluntary Action Indicated (VAI)Plant operations - Precautions (21 CFR 117.80(a))
Hazard Analysis - Identification of Hazard (21 CFR 117.130(a)(1))
Sanitation Controls Procedures (21 CFR 117.135(c)(3))
Reanalysis frequency (21 CFR 117.170)
and 1 more
May 8, 2019Voluntary Action Indicated (VAI)No citations listed
Jun 30, 2016Voluntary Action Indicated (VAI)Precluding contaminants (21 CFR 110.40(a))
Convey sewage (21 CFR 110.37(b)(2))
Drainage (21 CFR 110.37(b)(4))
Nov 17, 2010Voluntary Action Indicated (VAI)Materials and workmanship (21 CFR 110.40(a))
Storage of cleaned portable equipment (S) (21 CFR 110.35(e))
Lack of effective pest exclusion (21 CFR 110.35(c))
Glove condition (21 CFR 110.10(b)(5))
and 1 more

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.

DateClassRecallProduct and reason
Aug 20, 2018Class IIF-1908-2018Mexican Style Ricotta Cheese labeled, "Don Froylan Requeson***Mexican Style Ricotta…
Don Froylan Requeson is being recalled because the ingredient statement does not declare milk, a major food allergen. The pasteurized whey…
Jan 22, 2015Class IIF-1300-2015Queso Oaxaca Whole Milk Mozarella Cheese, Don Froylan brand, packaged in 12 oz., 1 lb…
Milk was not pasteurized properly
Feb 29, 2012Class IIF-1030-2012Don Froylan Queso Fresco, 12 oz. package. The UPC is 8 85790 00002 3. The product is…
The milk had not been adequately pasteurized before it was made into cheese.

FDA record score

4 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
RecordDatePoints x age weightAdds
Inspection classified VAISep 26, 20196 x 0.251.5
Inspection classified VAIMay 8, 20196 x 0.251.5
Class II recall F-1908-2018, this FEI as the recalling firmAug 20, 20184 x 0.251
Inspection classified VAIJun 30, 201610 years or older, so it adds no points0
Class II recall F-1300-2015, this FEI as the recalling firmJan 22, 201510 years or older, so it adds no points0
Class II recall F-1030-2012, this FEI as the recalling firmFeb 29, 201210 years or older, so it adds no points0
Inspection classified VAINov 17, 201010 years or older, so it adds no points0

When each source was last refreshed

FDA sources behind this page and when RegDataLab last refreshed each one
RecordsLast refreshedSource as ofStatus
InspectionsNov 14, 2026Newest record Nov 5, 2026Current
Inspection citationsNov 14, 2026Newest record Nov 5, 2026Current
Compliance actions (warning letters, injunctions and other action types)Nov 2, 2026Newest record Oct 29, 2026Current
Warning letter textNov 14, 2026Newest record Nov 10, 2026Current
Recalls (Enforcement Report)Nov 14, 2026Newest record Nov 11, 2026Current
Form 483s and inspection documentsNov 13, 2026Newest record Nov 12, 2026Current
Import refusalsNov 2, 2026Newest record Oct 22, 2026Current

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Facility details

Company
Ochoa's Queseria LLC
Location
Salem, OR (US)
Source
inspections

FDA data resources

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