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CH Guenther And Son, Inc. FDA Record

Warning letters, Form 483s, inspections, recalls and 510(k) clearances

CH Guenther And Son, Inc. has 0 FDA recalls, 4 inspections, 0 510(k) clearances and 0 compliance actions on record. No FDA warning letter addressed to "CH Guenther And Son, Inc." is on file.

What these totals cover: FDA records filed under the name "CH Guenther And Son, Inc." and its spelling variant "Ch Guenther And Son". Records filed under related names are not included; see Related names.

Latest recall: F-0702-2025 · Mar 11, 2025 · filed under C.H. Guenther And Son
Latest inspection: Mar 18, 2025 · NAI

Newer recall under related name C.H. Guenther And Son: Mar 11, 2025, F-0702-2025.

Summary

Record counts and when each FDA source was last refreshed
Records	Count	Last refreshed	Source as of	Status
Recalls	0	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	4	Nov 14, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA record by year

CH Guenther And Son, Inc.'s FDA inspections, warning letters and recalls in each of the last 10 calendar years (2017 to 2026, 2026 so far).

Year	Inspections	OAI	Warning letters	Recall records	Class I
2026	0	0	0	0	0
2025	1	0	0	0	0
2024	0	0	0	0	0
2023	1	0	0	0	0
2022	0	0	0	0	0
2021	0	0	0	0	0
2020	0	0	0	0	0
2019	0	0	0	0	0
2018	0	0	0	0	0
2017	0	0	0	0	0

Inspections are counted by the date they ended, warning letters by the date FDA issued them and recall records by the recall start date. FDA lists one recall record per recalled product, so one recall event can add several.

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Related names

Each name below has its own page. Its counts cover only the records FDA filed under that name and are not part of the totals for CH Guenther And Son, Inc. above.

Name	Relation	Recalls	510(k)	Inspections	Compliance actions	Most recent recall
C.H. Guenther And Son	Same company group	2	0	1	0	Mar 11, 2025 (F-0702-2025)

Recent FDA inspections

4 inspections from Oct 28, 2009 to Mar 18, 2025.

Date	Site	Product	Classification	FEI
Mar 18, 2025	Arlington, TX	Food/Cosmetics	No Action Indicated (NAI)	3009790116
Aug 2, 2023	Prosperity, SC	Food/Cosmetics	Voluntary Action Indicated (VAI)	3004349603
Oct 7, 2010	Salt Lake City, UT	Food/Cosmetics	No Action Indicated (NAI)	1720529
Oct 28, 2009	Salt Lake City, UT	Food/Cosmetics	No Action Indicated (NAI)	1720529

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

Look up the inspector observations behind these results with the FDA 483 search, or check for formal enforcement with the FDA warning letter search.

FDA-inspected facilities

3 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3009790116	Arlington, TX	1	Mar 18, 2025
FEI 3004349603	Prosperity, SC	1	Aug 2, 2023
FEI 1720529	Salt Lake City, UT	2	Oct 7, 2010

CH Guenther And Son, Inc. and the FDA: common questions

Has CH Guenther And Son, Inc. received an FDA warning letter?

No FDA warning letter addressed to the name "CH Guenther And Son, Inc." is on file. This answer covers that name only: letters addressed to a related company name or to one of its sites are listed on that name's or site's own page.

Has CH Guenther And Son, Inc. received an FDA Form 483?

FDA has not published a Form 483 for "CH Guenther And Son, Inc." in its reading room. FDA publishes some Form 483s, not all of them.

When did the FDA last inspect CH Guenther And Son, Inc.?

The most recent FDA inspection on file ended Mar 18, 2025 at Arlington, TX and was classified NAI. FDA has 4 inspections of CH Guenther And Son, Inc. on file.

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