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Schlotterbeck & Foss LLC FDA Inspection Record

FEI 3006534923 · Inspections, Form 483s, warning letters and import refusals

Schlotterbeck & Foss LLC is an FDA-inspected facility (FEI 3006534923) located in Chester, VT, US. RegDataLab tracks 7 FDA inspections at this facility.

What FDA found at this site

Latest inspection
Mar 20, 2025: No Action Indicated (NAI)
Inspections on record
7 (3 VAI, 4 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 Sep 10, 2021

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 20, 2025No Action Indicated (NAI)No citations listed
May 4, 2022No Action Indicated (NAI)No citations listed
Sep 17, 2019Voluntary Action Indicated (VAI)Plant construction and design (21 CFR 117.20(b))
Oct 27, 2016Voluntary Action Indicated (VAI)Floors, walls and ceilings (21 CFR 110.20(b)(4))
Reasonable precautions (21 CFR 110.80)
Raw materials, packaging, finished product (21 CFR 114.100(a))
Sep 2, 2014Voluntary Action Indicated (VAI)Q.C. instrument accuracy, maintenance (21 CFR 110.40(f))
As source of contamination (21 CFR 110.37(b)(3))
Storage (21 CFR 110.80(a)(1))
Raw materials, packaging, finished product (21 CFR 114.100(a))
and 1 more
Aug 18, 2011No Action Indicated (NAI)No citations listed
Jun 1, 2011No Action Indicated (NAI)No citations listed

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
Sep 10, 2021Class IIF-0070-2022Simply Nature Organic Poppy Seed Dressing
product may not be acidified
Sep 14, 2016Class IF-0677-2017Field Day Organic Ranch Dressing packaged in an 8 fl. oz. glass bottle, UPC #042563600242…
Undeclared milk and egg allergen.
Jul 29, 2016Class IIF-2237-2016SimplyNature Organic Chipotle Ranch Dressing, Net Wt. 12 FL OZ (354mL), UPC: 0 41498 21862…
Product contains undeclared wheat.

FDA record score

3 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.

6 records behind this number
RecordDatePoints x age weightAdds
Inspection classified VAISep 17, 20196 x 0.251.5
Class II recall F-0070-2022, this FEI as the recalling firmSep 10, 20214 x 0.251
Inspection classified VAIOct 27, 201610 years or older, so it adds no points0
Class I recall F-0677-2017, this FEI as the recalling firmSep 14, 201610 years or older, so it adds no points0
Class II recall F-2237-2016, this FEI as the recalling firmJul 29, 201610 years or older, so it adds no points0
Inspection classified VAISep 2, 201410 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
Schlotterbeck & Foss LLC
Location
Chester, VT (US)
Source
inspections

FDA data resources

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