FreshPoint Denver, Incorporated

FDA Regulatory Profile

FreshPoint Denver, Incorporated appears in FDA public data with 2 recalls — including 2 Class I (most serious) —, 0 510(k) clearances, 6 FDA inspections, and 0 compliance actions on record. Its most recent recall (F-0138-2025, Class I) was initiated on Oct 22, 2024. Its most recent FDA inspection ended on Dec 15, 2025 (Voluntary Action Indicated (VAI)).

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Summary

Total Recalls
2 (2 Class I)
510(k) Clearances
0
Inspections
6
Compliance Actions
0

Recent Recalls

NumberClassProductDate
F-0138-2025Class I154784 1 / 5LB IMPERIALFRESH PROC FAJITA GRN PEPRED PEP W All lot codesOct 22, 2024
F-0137-2025Class IItem Number PACK/SZ BRAND DESCRIPTION Lot Codes 082076 4/5 LBS IMPERIALFRESH PROC ONION YELLOW JULIEOct 22, 2024

Recent FDA Inspections

DateSiteProductClassificationFEI
Dec 15, 2025Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)3003711767
Mar 15, 2023Denver, COFood/CosmeticsNo Action Indicated (NAI)3003711767
Nov 9, 2016Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)3003711767
Mar 5, 2013Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)3003711767
Dec 4, 2009Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)3003711767
Oct 24, 2008Denver, COFood/CosmeticsVoluntary Action Indicated (VAI)3003711767

FDA Data Dashboard classifications: NAI (no action indicated), VAI (voluntary action indicated), OAI (official action indicated).