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Callisons Inc

FDA Regulatory Profile

Callisons Inc has 0 FDA recalls, 9 inspections, 0 510(k) clearances and 0 compliance actions on record.

What these totals cover: FDA records filed under the name "Callisons Inc" and its spelling variant "Callisons".

Latest inspection: Sep 25, 2024 · NAI

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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	9	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

FDA Record by Year

Callisons 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	0	0	0	0	0
2024	1	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	3	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.

Recent FDA Inspections

9 inspections from Oct 14, 2009 to Sep 25, 2024.

Date	Site	Product	Classification	FEI
Sep 25, 2024	Hamlet, IN	Food/Cosmetics	No Action Indicated (NAI)	3004277091
Aug 17, 2023	Sunnyside, WA	Food/Cosmetics	No Action Indicated (NAI)	3013376
Sep 27, 2018	Sunnyside, WA	Food/Cosmetics	No Action Indicated (NAI)	3013376
Mar 29, 2018	Hamlet, IN	Food/Cosmetics	No Action Indicated (NAI)	3004277091
Feb 1, 2018	Lacey, WA	Food/Cosmetics	No Action Indicated (NAI)	2000026847
Dec 22, 2015	Hamlet, IN	Food/Cosmetics	No Action Indicated (NAI)	3004277091
Mar 20, 2013	Hamlet, IN	Food/Cosmetics	No Action Indicated (NAI)	3004277091
Jun 7, 2011	Sunnyside, WA	Food/Cosmetics	No Action Indicated (NAI)	3013376
Oct 14, 2009	Chehalis, WA	Food/Cosmetics	No Action Indicated (NAI)	3011549

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.

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

4 inspected sites, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3004277091	Hamlet, IN	4	Sep 25, 2024
FEI 3013376	Sunnyside, WA	3	Aug 17, 2023
FEI 2000026847	Lacey, WA	1	Feb 1, 2018
FEI 3011549	Chehalis, WA	1	Oct 14, 2009

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