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Growland Inc

FDA Regulatory Profile

Growland Inc has 1 FDA recall, 1 inspection, 0 510(k) clearances and 0 compliance actions on record.

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

Latest recall: F-0648-2025 · Class II · Feb 18, 2025
Latest inspection: Apr 24, 2025 · 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	1	Nov 8, 2026	File dated Nov 3, 2026	Current
510(k) clearances	0	Nov 8, 2026	File dated Nov 2, 2026	Current
Inspections	1	Nov 13, 2026	Newest record Nov 5, 2026	Current
Compliance actions	0	Nov 2, 2026	Newest record Oct 29, 2026	Current

Recent recalls

1 recall record on Feb 18, 2025.

Number	Class	Product	Date
F-0648-2025	Class II	Dried Longan Pulp- Made in China, 8oz(227g), GROWLAND INC. rear panel- Organic Planted, Store in…	Feb 18, 2025

Recent FDA inspections

1 inspection on Apr 24, 2025.

Date	Site	Product	Classification	FEI
Apr 24, 2025	Chino, CA	Food/Cosmetics	No Action Indicated (NAI)	3014064807

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

1 inspected site, newest inspection first.

Facility	Location	Inspections	Latest
FEI 3014064807	Chino, CA	1	Apr 24, 2025

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